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Human Molecular Genetics Pages 1893-1899 © Oxford University Press
Unequal interchromosomal rearrangements may result in elastin gene deletions causing the Williams-Beuren syndrome
Introduction
Results
Discussion
Materials And Methods
Acknowledgements
References

Unequal interchromosomal rearrangements may result in elastin gene deletions causing the Williams-Beuren syndrome

Unequal interchromosomal rearrangements may result in elastin gene deletions causing the Williams-Beuren syndrome Fabrizio Dutly and Albert Schinzel*

Institut für Medizinische Genetik der Universität Zürich, Raemistrasse 74, CH-8001 Zürich, Switzerland

Received August 2, 1996; Revised and Accepted September 16, 1996

Williams-Beuren syndrome (WBS) is generally the consequence of an interstitial microdeletion at 7q11.23, which includes the elastin gene, thus causing hemizygosity at the elastin gene locus. The origin of the deletion has been reported by many authors to be maternal in ~60% and paternal in 40% of cases. Segregation analysis of grandparental markers flanking the microdeletion region in WBS patients and their parents indicated that in the majority of cases a recombination between grandmaternal and grandpaternal chromosomes 7 at the site of the deletion had occurred during meiosis in the parent from whom the deleted chromosome stemmed. Thus, the majority of deletions were considered a consequence of unequal crossing-over between homologous chromosomes 7 (interchromosomal rearrangement) while in the remaining cases an intrachromosomal recombination (between the chromatids of one chromosome 7) may have occurred. These results suggest that the majority of interstitial deletions of the elastin gene region occur during meiosis, due to unbalanced recombination while a minority could occur before or during meiosis probably due to intrachromosomal rearrangements. The recurrence risk of the interchromosomal rearrangements for sibs of a proband with non-affected parents must be negligible, which fits well with the observation of sporadic occurrence of almost all cases of WBS.

INTRODUCTION

The Williams-Beuren syndrome (WBS) is characterised by growth and mental retardation with a friendly, outgoing personality, dysmorphic facial features, hypercalcaemia in early infancy, and congenital cardiovascular malformations, in particular supravalvular aortic stenosis (1 -3 ). This, almost always sporadically occurring, disorder (incidence about 1/20 000 newborns) has been shown to result from a contiguous gene deletion syndrome comprising the elastin gene (4 ) and the recently located gene LIM-kinase 1 (5 ). Individuals with classic WBS have a chromosomal deletion >500 kb at 7q11.23 (5 ). Hemizygosity of the elastin gene is probably responsible for some of the characteristic features of the WBS, including supravalvular aortic stenosis, hoarse voice, and some of the WBS facial features. However, mental retardation and hypercalcaemia in WBS may indicate that hemizygosity of other genes adjacent to the elastin locus may also contribute to the phenotype.

The human elastin gene has been mapped to 7q11.23 (6 ). Indik et al. (7 -8 ) found a remarkable abundance of Alu repetitive sequences in the 3' region of the gene and several alternatively spliced isoforms.

Repetitive DNA sequences and Alu sequences flanking deletion breakpoints have been noted in a considerable number of human gene mutations which cause genetic disorders, including defects in the genes for [alpha]-globin (9 ), [beta]-globin (10 ), growth hormone (11 ) and many others. Such repeated and highly homologous sequences may facilitate a misalignment of chromosomes followed by an unequal crossing-over event which increases the homologous recombination and greatly enhances the possibility of a deletion. Mispairing between the repeats might result in the formation of a loop between the two repeats. Subsequent excision of the loop will remove the sequences between the two repeats. One might hypothesize that an unequal recombination involving Alu sequences at 7q11 would generate a deletion resulting in WBS. The particular mechanism(s) involved in rearrangements of proximal 7q remains to be elucidated by molecular analysis of breakpoint sites.


Figure 1.(A) Haplotype representation of chromosome 7 markers for WBS families with maternal (M) or paternal (P) deletion at the elastin gene. (B) Control families with normal (N) elastin gene. Alleles inherited from the grandmother are shown by hatched rectangles, markers inherited from the grandfather are shown by black rectangles. Closed circles represent uninformative markers.

In order to analyse the mechanisms underlying maternal and paternal de novo deletions in WBS, we performed a molecular study of 15 families. The parental origin of the deletion was first determined. Segregation analysis of 7q11-q21 markers in the 15 families with the available grandparents suggested that the deletions were in the majority due to an unequal interchromosomal rearrangement.

Table 1 Results of molecular markers studies around the elastin locus in 15 WBS families
Family

 Origin of

 Microsatellites
 

 deletion

 ELN MvaI

 ELN dinuc.

 D7S489

 D7S1870
5

 mat

 b,ab,ab

 b,bc,ab

 a,bb,aa

 b,ac,bb
9

 mat

 c,bc,ac

 a,ab,ab

 a,bb,aa

 b,aa,ab
35

 mat

 a,ab,ab

 c,ab,cc

 c,ab,bc
70

 mat

 a,bc,ab

 b,ab,bb
81

 mat

 a,bc,ac

 b,ab,ab

 a,bb,ac

 c,ab,cd
82

 mat

 c,ab,bc

 b,ab,bb

 a,bd,ac
84

 mat

 c,ac,bc

 a,bb,ab

 a,bb,ac
101

 mat

 a,ac,aa

 b,ac,bc

 b,aa,-

 b,ac,ab
3

 pat

 a,ab,cc

 c,cc,ab

 a,ab,bc
34

 pat

 b,ab,ac

 c,bc,ac

 c,cc,ab
38

 pat

 a,ab,ab

 a,ab,bb

 a,ab,ab
41

 pat

 b,ab,bb

 a,ab,bb

 a,ab,ab
52

 pat

 a,aa,cc

 c,ac,bb

 b,ab,bb
63

 pat

 c,ac,ab

 a,ac,bc

 a,aa,aa
76

 pat

 a,ab,aa

 b,bb,ab

 b,bc,ab

 b,bc,ad
The alleles are given in the order: patient, mother, father. Markers informative for the parental origin of the deletion are shown in bold. Pat, paternal deletion; mat, maternal deletion. Families 3, 5, 9, 34, 35, 38, 41, 52, 63, 70 and 76 were also reported by Robinson et al. (30).

RESULTS

The 15 WBS patients were genotyped for the elastin gene or for sequences flanking this gene. The absence of maternal or paternal contribution to the patients in at least one of these loci, demonstrated the origin of the deletion (Table 1 ). In eight cases there was no maternal inheritance of these markers, and in the other seven cases, there was lack of paternal alleles.

Fluorescent in situ hybridization (FISH) analysis of the parents, with the probe WSCR (ONCOR), demonstrated that all the deletions had occured de novo.

The 15 families consisting of the patient, the two parents and the available maternal or paternal grandparents were genotyped using microsatellites centromeric and telomeric adjacent to the elastin gene. The markers allowed us to determine which allele was inherited from the parents and from the grandparents. Haplotype analysis of the flanking markers on each side of the deletion showed a recombination event between the centromeric (D7S663, D7S645, D7S672, D7S653) and the telomeric loci (D7S669, D7S440, D7S634, D7S524, D7S630) in 10 out of the 15 analysed families (Fig. 1 A). As shown in Figure 2 A, in Family 5 the WBS patient inherited the allele `c' from the maternal grandfather for locus D7S672. The allele `c' for locus D7S669 was inherited from the maternal grandmother, suggesting a crossing-over between the two reported loci, which caused the deletion at the elastin gene. In contrast, in Family 82 (Fig. 2 B) the alleles `b' (at D7S672) and `d' (at D7S669) were inherited from the maternal grandmother. A recombination event between the grandmaternal and grandpaternal haplotypes in the deleted region is unlikely.


Figure 2. Results for the microsatellite loci D7S672, D7S669 and D7S504 in Family 5 (A) and Family 82 (B). The patient in Family 5 has inherited the grandpaternal allele c for D7S672 and the grandmaternal allele c for D7S669, indicating crossing-over between markers flanking the deletion region. The patient of Family 82 has inherited the grandmaternal alleles b and d for the loci D7S672 and D7S669, excluding crossing over, the grandpaternal allele d for D7S504. Lane 1, mother; lane 2, patient; lane 3, father; lane 4, maternal grandmother; lane 5, maternal grandfather.

Buetow et al. (12 ) showed that the elastin gene maps between D7S502 and D7S524. Biallelic inheritance was observed with the markers D7S663, D7S645, D7S672, D7S669, D7S440, D7S634 and D7S524 (Table 2 ), thus excluding hemizygosity at these loci for most of the WBS patients.


Table 2 Microsatellite analysis of chromosome 7 markers in 15 WBS families The order of the family members available for genotype analysis is always indicated under the family number. Allele designations (marked a-f) are arbitrary. P, patient; M, mother; F, father; GM, grandmother; GF, grandfather. Bold indicates allele inherited from the grandmother. Bold italic indicates allele inherited from the grandfather. Underline indicates biallelic inheritance for markers flanking the elastin gene.


Table 3 Microsatellite analysis of chromosome 7 markers in 12 control families The order of the family members for genotype analysis is always child, mother, father, grandmother, grandfather. Families C1-C5, paternal grandparents; C6-C12, maternal grandparents. Allele designations (marked a-f) are arbitrary. Bold indicates allele inherited from the grandmother. Bold italic indicates allele inherited from the grandfather.

These results indicate that unequal crossing-over between the two chromosomes 7 is the mechanism causing the interstitial deletions in the majority of cases of WBS with elastin deletions.

No recombination of markers around 7q11.23 could be detected in the control families, who had no deletion of the elastin gene (Table 3 and Fig. 1 B).

Since the 7q31-32 and 7p13 regions are frequently involved in rearrangements (12 ), we also investigated the recombination events occurring at the two telomeric ends. In seven WBS families we detected a second recombination event (Table 2 , Families 5, 9, 35, 70, 101, 3 and 38) with the markers D7S504, D7S550 and D7S559 mapping between 7q31 and 7qter. One family (84) did not show recombination for D7S559 and two families (41 and 63) were not informative. The results of analysis of the microsatellites D7S507, D7S513, D7S481 and D7S531 close to the 7pter region demonstrated an additional recombination in the short arm in Families 70, 84, 41 and 63. The five families (81, 82, 34, 52 and 76) with no evident crossing-over at the deleted region, showed recombination either at 7pter (Families 81 and 34) or 7qter (Families 81, 82, 52 and 76). Family 82 had a recombination starting at D7S504 (Fig. 2 B) for the 7q. Family 52 showed two recombinations, the first between D7S479 and D7S504, the second at D7S559 (Fig. 1 A). The same markers were used for the control families; eight showed recombination either at 7qter or at 7pter (Families C2, C6, C7, C8, C9, C10, C11 and C12). Families C1, C3 and C5 had a crossing-over between D7S524 and D7S479. The results for control families, indicate that the telomeric regions are more recombinogenic than the loci close to the elastin gene.

DISCUSSION

We have demonstrated that in 10 out of the 15 (67%) WBS families with a de novo deletion within 7q11.23, the segment flanking the deleted region contained recombined haplotypes. Therefore the deletion must be the result of an unequal crossing-over event between the chromosome 7 homologues during gametogenesis. An excess of meiotic recombination at 7q11.23 and at 7pter or 7qter, might partially explain the resulting deletion. The remaining five (33%) families showed no recombination at either side of the deletion. The genetic distance between D7S653 and D7S669 is 8 cM, and thus the probability of a double recombination is very low. It is possible that the deletions in the non-recombined families result from intrachromosomal rearrangements. Thus, elastin deletions causing the WBS might arise either by interchromosomal events (unequal crossing-over) or by intrachromosomal rearrangements. No sex specific occurrence of intra- or interchromosomal rearrangements was demonstrated (2/8 for maternal WBS, 3/7 for paternal WBS). This is in contrast with the preponderance of unequal crossing-over in males and the preponderance of intrachromosomal deletion occurring in females as proposed by Leguern et al. (14 ) for hereditary neuropathy with liability to pressure palsies (HNPP).

Meiosis is the basis for the production of haploid gametes from diploid cells, allowing sexual reproduction in eukaryotic organisms. Meiotic cells undergo DNA replication followed by the establishment of physical connections between homologous chromosomes. Paired chromosomes undergo genetic recombination followed by reductional division at meiosis I. The mechanism of meiotic recombination includes reciprocal breakage, exchange of DNA segments and rejoining of chromatids.

On the basis of observed recombination frequencies, meiotic recombination does not occur randomly along chromosomes, but seems to be more or less frequent in specific regions. The structure of chromatin is directly involved in recombination as demonstrated by lack of crossing-over in highly condensed heterochromatin (15 ). Unequal recombinations are mediated by related gene sequences or repetitive sequence elements, as proposed by the presence of repetitive DNA sequences and Alu sequences flanking deletion breakpoints in many human genetic disorders (9 -11 ). Misaligned non-sister chromatids during meiosis and misaligned sister chromatids, followed by excision of a chromatid loop, have also been proposed as a mechanism for deletions of several Mb such as those in the Prader-Willi/Angelman syndrome (16 ) and HNPP (14 ). The most abundant repetitive elements in the human genome are the Alu repeats, they have also been shown to be involved in a considerable number of human gene deletions (17 -25 ).

The human elastin gene has relatively large introns which are characterized by Alu repetitive elements clustered at the 3' end (7 ). The presence of repetitive elements might facilitate chromosome 7 misalignment in the elastin gene region. Furthermore, the breakpoints in the LIM-kinase1 gene, which is adjacent to elastin and directly involved in the partial WBS phenotype, seem to occur within Alu repeats (5 ). This finding strengthens the argument that Alu sequences are involved in unequal recombination leading to WBS deletion. Additional work is required to characterize the precise sequence at the deletion breakpoints of classical WBS (>500 kb), in order to determine the pathogenetic mechanism(s) that cause these (and other) deletions.

Unequal crossing-over during meiosis was also suggested as a mechanism generating DNA duplication on chromosome 17 causing Charcot-Marie-Tooth disease, and the deletion in the same region causing HNPP (26 ). Duplications and deletions have been also described in the LDL receptor gene (17 ). For the elastin gene or the 7q11.2 region there is no description of patients with a duplication. In addition to the difficulty in detecting such a duplication with an unknown phenotype, it is possible that the corresponding duplication is either not associated with an abnormal phenotype or that it is lethal.

In the control families, recombinations had mainly occurred at the two chromosome 7 telomeres and not at the elastin locus. Genotyping of these few control families seems to suggest that the chromosome segment 7q11 is not especially prone to recombination. It may be expected that a lower recombination frequency occurs in regions where an intact structure of both alleles must be maintained for correct gene expression.

A practical consequence of our findings is that they can improve prediction of recurrence risk for sibs of an affected proband. If a recombination around the deleted segment can be demonstrated, the deletion must have occurred during meiosis; mitotic recombination is extremely unlikely, and thus the recurrence risk will be virtually zero. In case of a presumed intrachromosomal recombination, an unlikely premeiotic origin cannot be fully excluded. Thus, the possibility of gonadal mosaicism for the deletion has to be considered, with the recurrence risk possibly being in the range of 1-2%. Occurrence of WBS in sibs of unaffected parents has been reported earlier (27 ), but to the best of our knowledge has never been reported in cases with proven elastin deletion. On the other hand, there is one report of a 22q11.22 microdeletion in sibs of non-deleted parents (28 ). It would be interesting to investigate this family for recombinations around the deletion.

Prader-Willi/Angelman syndrome and CATCH22, like WBS, are genetic diseases characterized by interstitial deletions close to the centromere. Segregation analysis using markers flanking the microdeletion region in these three conditions might provide further information as to whether a common mechanism is responsible for interstitial deletions.

MATERIALS AND METHODS

The patients were selected from a series of WBS patients investigated with microsatellite markers and FISH at the Institute of Medical Genetics of the University of Zürich; clinical and molecular data have been reported by Kotzot et al. (29 ) and Robinson et al. (30 ).

DNA was extracted from peripheral blood of the probands with WBS, from each parent, and from the grandparents from the side of the deletion origin, using standard methods.

The following microsatellites with the indication of genetic order and distance (cM) were used: 7pter-D7S531-(11)-D7S481-(11)- D7S513-(8)-D7S507-(51)-D7S499-(3)-D7S663-(3)-D7S645-(3)-D7S672-(1)-D7S653-(1.8)-ELN-(6)-D7S669-(2.4)-D7S440-(0.6)-D7S634-(6)-D7S524-(2)-D7S630-(3)-D7S492-(9)-D7S479-(26)-D7S504-(51)-D7S550-(4)-D7S559-7qter (31).

The following markers were used in order to determine the origin of the deletion: (i) ELN MvaI, the amplified products of exon 20 of the elastin gene were digested with MvaI as described (32 ); (ii) ELN dinuc., which maps near exon 18 within the elastin gene (33 ); (iii) D7S1870 and D7S489 with an informativity of 85% for detecting deletions at 7q11.23 (34 ). All primers were obtained from Research Genetics, with the exception of ELN MvaI, which was synthesized elsewhere.

Between 200 and 500 ng of DNA were amplified with the indicated primers for chromosome 7 in a volume of 25 [mu]l. PCR amplification was performed on a Perkin-Elmer 9600 with 32 cycles of 30 s at 94oC, 45 s at 55-60oC for the annealing, and 80 s at 72oC for the extension. The reaction product was mixed in an equal volume of urea loading buffer (42% urea, 0.1% xylene cyanol, 0.1% bromphenol blue, and 0.1% 0.5 M EDTA) and was loaded onto a 0.4 mm thick 6% polyacrylamide/50% urea gel. Visualization of bands was done by silver staining of the gels.

ACKNOWLEDGEMENTS

We would like to thank all the families involved in this study and their physicians for their cooperation. This project was supported by the Swiss National Foundation grant no. 32-37798.93.

REFERENCES

1 Williams,J.C.P., Barrat-Boyers,B.G. and Lowe,J.B. (1961) Supravalvular aortic stenosis. Circulation, 24, 1311-1318.

2 Beuren,A.J., Apitz,J. and Armjanz,D. (1962) Supravalvular aortic stenosis in association with mental retardation and facial appearance. Circulation, 26, 1235-1240.

3 Jones,K.L. and Smith,D.W. (1975) The Williams elfin facies syndrome: a new perspective. J. Pediatr., 86, 718-723. MEDLINE Abstract

4 Ewart,A.K., Morris,C.A., Atkinson,D., Jin,W., Sternes,K., Spallone,P., Stock,A.D., Leppert,M. and Keating,M.T. (1993) Hemizygosity at the elastin locus in a developmental disorder, Williams-Beuren syndrome. Nature Genet., 5, 11-16 MEDLINE Abstract

5 Frangiskakis,J.M., Ewart,A.K., Morris,C.A., Mervis,C.B., Bertrand,J., Robinson,B.F., Klein,B.P., Ensing,G.J., Everett,L.A., Green,E.D., Pröschel,C., Gutowski,N.J., Noble,M., Antkinson,D.L., Odelberg,S.J. and Keating,M.T. (1996) LIM-kinase 1 hemizygosity implicated in impaired visuospatial constructive cognition. Cell, 86, 59-69. MEDLINE Abstract

6 Fazio,M.J.,Mattei,M.G., Passage,E., Chu,M.L., Black,D., Solomon,E., Davidson,J.M. and Uitto,J. (1991) Human elastin gene: new evidence for localization to the long arm of chromosome 7. Am. J. Hum. Genet., 48, 696-703. MEDLINE Abstract

7 Indik,Z., Yoon,K., Morrow,S.D., Cicila,G., Rosenbloom,J.C., Rosenbloom,J. and Ornstein-Goldstein,N. (1987) Structure of the 3-prime region of the human elastin gene: great abundance of Alu repetitive sequences and few coding sequences. Connect. Tissue Res., 16, 197-211. MEDLINE Abstract

8 Indik,Z., Yeh,H., Ornstein-Goldstein,N., Kucich,U., Abrams,W., Rosenbloom,J.C. and Rosenbloom,J. (1989) Structure of the elastin gene and alternative splicing of elastin mRNA: implication for human desease. Am. J. Med. Genet., 34, 81-90. MEDLINE Abstract

9 Nicholls,R.D., Fischel-Ghodsian,N. and Higgs,D.R. (1987) Recombination at the human alpha globin gene cluster: sequence features and topological constrains. Cell, 49, 369-378. MEDLINE Abstract

10 Henthorn,P.S., Mager,D.L., Huisman,T.H.J. and Smithies,O. (1986) A gene deletion ending within a complex array of repeated sequences 3' to the human [beta]-globin gene cluster. Proc. Natl. Acad. Sci. USA, 83, 5194-5198. MEDLINE Abstract

11 Vnençak-Jones,C.L. and Phillips,J.A. III (1990) Hotspots for growth hormone gene deletions in homologous regions outside of Alu repeats. Science, 250, 1745-1748. MEDLINE Abstract

12 Buetow,K.H., Weber,J.L., Ludwingsen,S, Scherpbier-Heddema,T., Duyk,G.M., Sheffield,V.C., Wang,Z. and Murray,J.C. (1994) Integrated human genomic-wide maps constructed using CEPH reference panel. Nature Genet., 6, 391-393. MEDLINE Abstract

13 Tsui,L.C., Donis-Keller,H. and Grzeschik,K.H. (1995) Report of the second international workshop on human chromosome 7 mapping 1994. Cytogenet. Cell Genet., 71, 2-21. MEDLINE Abstract

14 Leguern,E., Gouider,R., Ravisé,N., Lopes,J., Tardieu,S., Gugenheim,M., Abbas,N., Bouche,P., Agid,Y and Brice,A. (1996) A de novo case of hereditary neuropathy with liability to pressure palsies (HNPP) of maternal origin: a new mechanism for deletion in 17p11.2? Hum. Mol. Genet., 5, 103-106. MEDLINE Abstract

15 McKee,B.D. and Hunt,M.A. (1993) Sex chromosomes, recombination, and chromatin conformation. Chromosoma, 102, 71-80. MEDLINE Abstract

16 Nicholls,R.D. (1994) Recombination model for generation of a submicroscopic deletion in familial Angelman syndrome. Hum. Mol. Genet., 3, 9-11. MEDLINE Abstract

17 Lehrman,M.A., Goldstein,J.L., Russell,D.W. and Brown,M.S. (1987) Duplication of seven exons in LDL receptor gene caused by Alu-Alu recombination in a subject with familial hypercholesterolemia. Cell, 48, 827-835. MEDLINE Abstract

18 Rouyer,F., Simmler,M.C., Page,D.C. and Weissenbach,J. (1987) A sex chromosome rearrangement in a human XX male caused by Alu-Alu recombination. Cell, 51, 417-425. MEDLINE Abstract

19 Li,L. and Bray,P.F. (1993) Homologous recombination among three intragene sequences causes an inversion-deletion resulting in the hereditary bleeding disorder Glanzmann thrombasthenia. Am. J. Hum. Genet., 53, 140-149. MEDLINE Abstract

20 Nehls,M., Schorpp,M. and Boehm,T (1995) An intragenic deletion in the human PTPN6 gene affects transcriptional activity. Hum. Genet., 95, 713-715. MEDLINE Abstract

21 Hori,T., Tomatsu,S., Nakashima,Y., Uchiyama,A., Fukuda,S., Sukegawa,K. Shimozawa,N., Suzuki,Y., Kondo,N., Horiuchi,T., Ogura,S. and Orii,T. (1995) Mucopolysaccharidosis type IVA: common double deletion in the N-acetylgalactosamine-6-sulfatase gene (GALNS). Genomics, 26, 535-542. MEDLINE Abstract

22 Jalanco,A., Manninen,T. and Peltonen,L. (1995) Deletion of the C-terminal end of aspartylglucosaminidase resulting in a lysosomal accumulation disease: evidence for a unique genomic rearrangement. Hum. Mol. Genet., 4, 435-441.

23 Wang,I., Weil,D., Levilliers,J., Affara,N.A., de la Chapelle,A. and Petit,C. (1995) Prevalence and molecular analysis of two hot spots for ectopic recombination leading to XX maleness. Genomics, 28, 52-58. MEDLINE Abstract

24 Hobbs,H.H., Brown,M.S., Goldstein,J.L. and Russel,D.W. (1986) Deletion of exon encoding cysteine-rich repeat of low-density lipoprotein receptor alerts its binding specificity in a subject with familial hypercholesterolemia. J. Biol. Chem., 261, 13114-13120. MEDLINE Abstract

25 Horsthemke,B., Beisiegel,U., Dunning,A., Havinga,J.R., Williamson,R. and Humphries,S. (1987) Unequal crossing-over between two Alu-repetitive DNA sequences in the low-density-lipoprotein-receptor gene. Eur. J. Biochem., 164, 77-81. MEDLINE Abstract

26 Chance,P.F., Alderson,M.K., Leppig,K.A., Lensch,M.W., Matsunami,N., Smith,B., Swanson,P.D., Odelberg,S.J., Disteche,C.M. and Bird,T.D. (1993) DNA deletion associated with hereditary neuropathy with liability to pressure palsies. Cell, 72, 143-151. MEDLINE Abstract

27 Burn, J. (1986) Williams syndrome. J. Med. Genet., 23, 389-395. MEDLINE Abstract

28 Eydoux,P., Kasprzak,L., Elliott,A.M. and Der Kaloustian,V.M. (1995) De novo deletion of 22q11 in two male siblings with different phenotypes. Am. J. Hum. Genet., 57, A113.

29 Kotzot,D., Bernasconi,F., Brecevic,L., Robinson,W.P., Kiss,P., Kosztolany,G., Lurie,I.W., Superti-Furga,A. and Schinzel,A. (1995) Phenotype of the Williams-Beuren syndrome associated with hemizygosity at the Elastin locus. Eur. J. Pediatr., 154, 477-482. MEDLINE Abstract

30 Robinson,W.P., Waslynka,J., Bernasconi,F., Wang,M., Clark,S., Kotzot,D. and Schinzel,A. (1996) Delineation of 7q11.2 deletions associated with Williams-Beuren syndrome and mapping of a repetitive sequence to within and to either side of the common deletion. Genomics, 34, 17-23. MEDLINE Abstract

31 Gyapay,G., Morissette,J., Vignal,A., Dib,C., Fizames,C., Millasseau,P., Marc,S., Bernardi,G., Lathrop,M. and Weissenbach,J. (1994). The 1993-1994 Généthon human genetic linkage map. Nature Genet., 7, 246-339. MEDLINE Abstract

32 Tromp,G., Christiano,A., Indik,Z., Boyd,C, Rosenbloom,J, Deak,S., Prockop,D. and Kuivaniemi,H. (1991) A to G polymorphism in ELN gene. Nucleic Acids Res., 19, 4314.

33 Foster,K., Ferrell,R., King-Underwood,L., Povey,S., Attwood,J., Rennick,R., Humphries,S.E. and Henney,A.M. (1993) Description of a dinucleotide repeat polymorphism in the human elastin gene and its use to confirm assignment of the gene to chromosome 7. Ann. Hum. Genet., 57, 87-96. MEDLINE Abstract

34 Gilbert-Dussardier,B., Bonneau,D., Gigarel,N., Le Merrer,M., Bonnet,D., Philip,N., Serville,F., Verloes,A., Rossi,A., Aymé,S.,Weissenbach, J., Mattei,M.G., Lyonnet,S. and Munnich,A. (1995) A novel microsatellite DNA marker at locus D7S1870 detects hemizygosity in 75% of patients with Williams syndrome. Am. J. Hum. Genet., 56, 544-547.

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S. C. Saitta, S. E. Harris, A. P. Gaeth, D. A. Driscoll, D. M. McDonald-McGinn, M. K. Maisenbacher, J. M. Yersak, P. K. Chakraborty, A. M. Hacker, E. H. Zackai, et al.
Aberrant interchromosomal exchanges are the predominant cause of the 22q11.2 deletion
Hum. Mol. Genet., February 15, 2004; 13(4): 417 - 428.
[Abstract] [Full Text] [PDF]

Home page
 Hum Mol GenetHome page
M. Tassabehji
Williams-Beuren syndrome: a challenge for genotype-phenotype correlations
Hum. Mol. Genet., October 15, 2003; 12(90002): R229 - 237.
[Abstract] [Full Text] [PDF]

Home page
 J. Med. Genet.Home page
R Heller, A Rauch, S Luttgen, B Schroder, and A Winterpacht
Partial deletion of the critical 1.5 Mb interval in Williams-Beuren syndrome
J. Med. Genet., August 1, 2003; 40(8): e99 - 99.
[Full Text] [PDF]

Home page
 JCBHome page
F.-M. Deng, F.-X. Liang, L. Tu, K. A. Resing, P. Hu, M. Supino, C.-C. A. Hu, G. Zhou, M. Ding, G. Kreibich, et al.
Uroplakin IIIb, a urothelial differentiation marker, dimerizes with uroplakin Ib as an early step of urothelial plaque assembly
J. Cell Biol., November 25, 2002; 159(4): 685 - 694.
[Abstract] [Full Text] [PDF]

Home page
 GeneticsHome page
V. L. Browning, R. A. Bergstrom, S. Daigle, and J. C. Schimenti
A Haplolethal Locus Uncovered by Deletions in the Mouse t Complex
Genetics, February 1, 2002; 160(2): 675 - 682.
[Abstract] [Full Text] [PDF]

Home page
 Hum Mol GenetHome page
D. Naf, L. A. Wilson, R. A. Bergstrom, R. S. Smith, N. C. Goodwin, A. Verkerk, G. J. van Ommen, S. L. Ackerman, W. N. Frankel, and J. C. Schimenti
Mouse models for the Wolf-Hirschhorn deletion syndrome
Hum. Mol. Genet., January 1, 2001; 10(2): 91 - 98.
[Abstract] [Full Text] [PDF]

Home page
 J. Med. Genet.Home page
D. TROST, W. WIEBE, S. UHLHAAS, P. SCHWINDT, and G. SCHWANITZ
Investigation of meiotic rearrangements in DGS/VCFS patients with a microdeletion 22q11.2
J. Med. Genet., June 1, 2000; 37(6): 452 - 454.
[Full Text]

Home page
 Genome ResHome page
Y. Ji, E. E. Eichler, S. Schwartz, and R. D. Nicholls
Structure of Chromosomal Duplicons and their Role in Mediating Human Genomic Disorders
Genome Res., May 1, 2000; 10(5): 597 - 610.
[Abstract] [Full Text]

Home page
 FASEB J.Home page
N. PEZZI, I. PRIETO, L. KREMER, L. A. PÉREZ JURADO, C. VALERO, J. DEL MAZO, C. MARTÍNEZ-A, and J. L. BARBERO
STAG3, a novel gene encoding a protein involved in meiotic chromosome pairing and location of STAG3-related genes flanking the Williams-Beuren syndrome deletion
FASEB J, March 1, 2000; 14(3): 581 - 592.
[Abstract] [Full Text]

Home page
 Hum Mol GenetHome page
M. O. Dorschner, V. P. Sybert, M. Weaver, B. A. Pletcher, and K. Stephens
NF1 microdeletion breakpoints are clustered at flanking repetitive sequences
Hum. Mol. Genet., January 1, 2000; 9(1): 35 - 46.
[Abstract] [Full Text] [PDF]

Home page
 Arch. Dis. Child.Home page
K METCALFE
Williams syndrome: an update on clinical and molecular aspects
Arch. Dis. Child., September 1, 1999; 81(3): 198 - 200.
[Full Text]

Home page
 Genome ResHome page
U. DeSilva, H. Massa, B. J. Trask, and E. D. Green
Comparative Mapping of the Region of Human Chromosome 7 Deleted in Williams Syndrome
Genome Res., May 1, 1999; 9(5): 428 - 436.
[Abstract] [Full Text]

Home page
 Genome ResHome page
E. A. Carver and L. Stubbs
Zooming in on the Human-Mouse Comparative Map: Genome Conservation Re-examined on a High-Resolution Scale
Genome Res., December 1, 1997; 7(12): 1123 - 1137.
[Abstract] [Full Text] [PDF]

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