Hum. Mol. Genet. -- Table of Contents (2 [7] )

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Contents: Volume 2, Number 7   July 1993   [Index by Author]

       COMMENTARIES

       ORIGINAL ARTICLES

       SHORT REPORTS

       MUTUAL REPORTS

       MUTATION REPORTS

       DNA MARKERS AND POLYMORPHISMS

       NEW HUMAN DNA POLYMORPHISMS

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COMMENTARIES:

Anna-Maria Frischauf: Positional cloning uncovers a new old oncogene
Hum. Mol. Genet. 1993 2: 847-848; doi:10.1093/hmg/2.7.847 [PDF] [Request Permissions]

Keith Johnson: Malignant hyperthermia hots up!
Hum. Mol. Genet. 1993 2: 849; doi:10.1093/hmg/2.7.849 [PDF] [Request Permissions]

ORIGINAL ARTICLES:

Helen Donis-Keller, Shenshen Dou, David Chi, Katrin M. Carlson, Koji Toshima, Terry C. Lairmore, James R. Howe, Jeffrey F. Moley, Paul Goodfellow, and Samuel A. Wells, Jr: Mutations in the RET proto-oncogene are associated with MEN 2A and FMTC
Hum. Mol. Genet. 1993 2: 851-856; doi:10.1093/hmg/2.7.851 [Abstract] [PDF] [Request Permissions]

R. Sudbrak, A. Golla, K. Hogan, P. Powers, R. Gregg, I.Du Chesne, F. Lehmann-Horn, and T. Deufel: Exclusion of malignant hyperthermia susceptibility (MHS) from a putative MHS2 locus on chromosome 17q and of the ${alpha}$ 1, ß1, and ${gamma}$ subunits of the dihydropyridine receptor calcium channel as candidates for the molecular defect
Hum. Mol. Genet. 1993 2: 857-862; doi:10.1093/hmg/2.7.857 [Abstract] [PDF] [Request Permissions]

David E. lles, Bart Segers, Robert C.A. Sengers, Koen Monsieurs, Luc Heytens, P.Jane Halsall, Philip M. Hopkins, F.Richard Ellis, Julle L. Hall-Curran, Alistair D. Stewart, and Berend Wieringa: Genetic mapping of the ß₁- and ${gamma}$ -subunits of the human skeletal muscle L-type voltage-dependent calcium channel on chromosome 17q and exclusion as candidate genes for malignant hyperthermia susceptibility
Hum. Mol. Genet. 1993 2: 863-868; doi:10.1093/hmg/2.7.863 [Abstract] [PDF] [Request Permissions]

Timothy M. Olson, Virginia V. Michels, Noralane M. Lindor, Gregory M. Pastores, JamesL. Weber, DanielJ. Schaid, David J. Driscoll, Robert H. Feldt, and Stephen N. Thibodeau: Autosomal dominant supravalvular aortic stenosis: localization to chromosome 7
Hum. Mol. Genet. 1993 2: 869-873; doi:10.1093/hmg/2.7.869 [Abstract] [PDF] [Request Permissions]

Rajendra Kumar-Singh, G.Jane Farrar, Fiona Mansergh, Paul Kenna, Shoml Bhattacharya, Andreas Gal, and Peter Humphries: Exclusion of the involvement of all known Retinitis Pigmentosa loci in the disease present in a family of Irish origin provides evidence for a sixth autosomal dominant locus (RP8)
Hum. Mol. Genet. 1993 2: 875-878; doi:10.1093/hmg/2.7.875 [Abstract] [PDF] [Request Permissions]

Frances M. Richards, Maude E. Phipps, Farida Latlf, Masahlro Yao, Paul A. Crossey, Kelth Foster, W. Marston Llnehan, Nabeel A. Affara, Michael I. Lerman, Berton Zbar, Malcolm A. Ferguson-Smith, and Eamonn R. Maher: Mapping the Von Hippel — Lindau disease tumour suppressor gene: identification of germline deletions by pulsed field gel electrophoresis
Hum. Mol. Genet. 1993 2: 879-882; doi:10.1093/hmg/2.7.879 [Abstract] [PDF] [Request Permissions]

Kathleen A. Lepplg, Carolyn J. Brown, Steven L. Bressler, Karen Gustashaw, Roberta A. Pagon, Huntington F. Willard, and Christine M. Disteche: Mapping of the distal boundary of the X-inactivation center in a rearranged X chromosome from a female expressing XIST
Hum. Mol. Genet. 1993 2: 883-887; doi:10.1093/hmg/2.7.883 [Abstract] [PDF] [Request Permissions]

Jlan Zuo, Carolyn Robblns, Slamak Bahariloo, David R. Cox, and Richard M. Myers: Construction of cosmid contigs and high-resolution restriction mapping of the Huntington disease region of human chromosome 4
Hum. Mol. Genet. 1993 2: 889-899; doi:10.1093/hmg/2.7.889 [Abstract] [PDF] [Request Permissions]

J.M. Rommens, B. Lin, G.B. Hutchinson, S.E. Andrew, Y.P. Goldberg, M.L. Glaves, R. Graham, V. Lal, J. McArthur, J. Nasir, J. Theilmann, H. McDonald, M. Kalchman, L.A. Clarke, K. Schappert, and M.R. Hayden: A transcription map of the region containing the Huntington disease gene
Hum. Mol. Genet. 1993 2: 901-907; doi:10.1093/hmg/2.7.901 [Abstract] [PDF] [Request Permissions]

M. Litt, P. Kramer, X.Y. Hauge, J.L. Weber, Z. Wang, P.J. Wilkle, M.S. Holt, S. Mishra, H. Donis-Keller, L. Warnich, A.E. Retief, C. Jones, and J. Welssenbach: A microsatellite-based index map of human chromosome 11
Hum. Mol. Genet. 1993 2: 909-913; doi:10.1093/hmg/2.7.909 [Abstract] [PDF] [Request Permissions]

Isabel M.Hanson, Anne Seawright, Karen Hardman, Shirley Hodgson, Dmitri Zaletayev, Gyorgy Fekete, and Veronica van Heyningen: PAX6 mutations in aniridia
Hum. Mol. Genet. 1993 2: 915-920; doi:10.1093/hmg/2.7.915 [Abstract] [PDF] [Request Permissions]

Valerie Greger, Elizabeth Woolf, and Marc Lalande: Cloning of the breakpoints of a submicroscopic deletion in an Angelman syndrome patient
Hum. Mol. Genet. 1993 2: 921-924; doi:10.1093/hmg/2.7.921 [Abstract] [PDF] [Request Permissions]

Philip Paul, Tom Letteboer, Larry Gelbert, Joanna Groden, Ray White, and Max J. Coppes: Identical APC exon 15 mutations result in a variable phenotype in familial adenomatous polyposis
Hum. Mol. Genet. 1993 2: 925-931; doi:10.1093/hmg/2.7.925 [Abstract] [PDF] [Request Permissions]

Carolin Lackner, Jonathan C. Cohen, and Helen H. Hobbs: Molecular definition of the extreme size polymorphism in apolipoprotein(a)
Hum. Mol. Genet. 1993 2: 933-940; doi:10.1093/hmg/2.7.933 [Abstract] [PDF] [Request Permissions]

Yves Labelle, Daniel Phaneuf, Barbara Leclerc, and Robert M.Tanguay: Characterization of the human fumarylacetoacetate hydrolase gene and identification of a missense mutation abolishing enzymatic activity
Hum. Mol. Genet. 1993 2: 941-946; doi:10.1093/hmg/2.7.941 [Abstract] [PDF] [Request Permissions]

Martin C. Wapenaar, Maria T. Bassl, Laura Schaefer, Alessandra Grillo, Giovanni B. Ferrero, A.Craig Chlnault, Andrea Ballabio, and Huda Y. Zoghbi: The genes for X-linked ocular albinism (OA1) and microphthalmia with linear skin defects (MLS): cloning and characterization of the critical regions
Hum. Mol. Genet. 1993 2: 947-952; doi:10.1093/hmg/2.7.947 [Abstract] [PDF] [Request Permissions]

N.German Pasterls, Barbara J.Trask, Susan Sheldon, and Jerome L.Gorskl: Discordant phenotype of two overlapping deletions involving the PAX3 gene in chromosome 2q35
Hum. Mol. Genet. 1993 2: 953-959; doi:10.1093/hmg/2.7.953 [Abstract] [PDF] [Request Permissions]

Lygia Pereira, Marina D'Alessio, Francesco Ramirez, Jennifer R.Lynch, Bryan Sykes, Theresa Pangilinan, and Jeffrey Bonadio: Genomic organization of the sequence coding for fibrillin, the defective gene product in Marfan syndrome
Hum. Mol. Genet. 1993 2: 961-968; doi:10.1093/hmg/2.7.961 [Abstract] [PDF] [Request Permissions]

Carmel M.McConville, Philip J.Byrd, Helen J.Ambrose, Tanja Stankovic, Yael Ziv, Anat Bar-Shira, Lina Vanagaite, Galit Rotman, Yosef Shiloh, Godfrey T.Gillett, John H.Riley, and A.Malcolm R.Taylor: Paired STSs amplified from radiation hybrids, and from associated YACs, identify highly polymorphic loci flanking the ataxia telangiectasia locus on chromosome 11q22–23
Hum. Mol. Genet. 1993 2: 969-974; doi:10.1093/hmg/2.7.969 [Abstract] [PDF] [Request Permissions]

Véronique Blanquet, Catherine Turleau, Marie-Sylvie Gross, Michel Goossens, and Claude Besmond: Identification of germline mutations in the RB1 gene by denaturant gradient gel electrophoresis and polymerase chain reaction direct sequencing
Hum. Mol. Genet. 1993 2: 975-979; doi:10.1093/hmg/2.7.975 [Abstract] [PDF] [Request Permissions]

M. Upadhyaya, P. Jardine, J. Maynard, J. Farnham, M. Sarfarazi, C. Wijmenga, J.E. Hewitt, R. Frants, P.S. Harper, and P.W. Lunt: Molecular analysis of British facioscapulohumeral dystrophy families for 4q DNA rearrangements
Hum. Mol. Genet. 1993 2: 981-987; doi:10.1093/hmg/2.7.981 [Abstract] [PDF] [Request Permissions]

David H.Gutmann, Lone B.Andersen, Jeffery L.Cole, Manju Swaroop, and Francis S.Collins: An alternatively-spliced mRNA in the carboxy terminus of the neurofibromatosis type 1 (NF1) gene is expressed in muscle
Hum. Mol. Genet. 1993 2: 989-992; doi:10.1093/hmg/2.7.989 [Abstract] [PDF] [Request Permissions]

Annett Behn-Krappa and Walter Doerfler: The state of DNA methylation in the promoter and exon 1 regions of the human gene for the interleukin-2 receptor ${alpha}$ chain (IL-2R ${alpha}$ ) in various cell types
Hum. Mol. Genet. 1993 2: 993-999; doi:10.1093/hmg/2.7.993 [Abstract] [PDF] [Request Permissions]

Victor E.Laubach, W.John Ryan, and Mark Brantly: Characterization of a human ${alpha}$ 1-antitrypsin null allele involving aberrant mRNA splicing
Hum. Mol. Genet. 1993 2: 1001-1005; doi:10.1093/hmg/2.7.1001 [Abstract] [PDF] [Request Permissions]

Michele Ramsay, Robert Williamson, Xavier Estivill, Brandon J. Wainwright, Meng-Falt Ho, Stephanie Halford, Juha Kere, Erkki Savilahti, Albert de la Chapelle, Marianne Schwartz, Martin Schwartz, Maurice Super, Peter Farndon, Carol Hardlng, Linda Meredith, Layla Al-Jader, Claude Ferec, Mirellle Claustres, Teresa Casals, Virginia Nunes, Paolo Gasparini, Anna Savoia, Pier Franco Pignatti, Giuseppe Novelli, Massimo Bennarelli, Bruno Dallapiccola, Luba Kalaydjieva, and Peter J. Scambler: Haplotype analysis to determine the position of a mutation among closely linked DNA markers
Hum. Mol. Genet. 1993 2: 1007-1014; doi:10.1093/hmg/2.7.1007 [Abstract] [PDF] [Request Permissions]

Núria Morral, Virginia Nunes, Teresa Casals, Miguel Chillón, Javier Giménez, Jaume Bertranpetit, and Xavier Estivill: Microsatellite haplotypes for cystic fibrosis: mutation frameworks and evolutionary tracers
Hum. Mol. Genet. 1993 2: 1015-1022; doi:10.1093/hmg/2.7.1015 [Abstract] [PDF] [Request Permissions]

Wilson J.Wall, Robert Williamson, Mary Petrou, Dla Papaioannou, and Brian H.Parkin: Variation of short tandem repeats within and between populations
Hum. Mol. Genet. 1993 2: 1023-1029; doi:10.1093/hmg/2.7.1023 [Abstract] [PDF] [Request Permissions]

Kenshi Komatsu, Tohru Ohta, Yoshihiro Jinno, Norio Nlikawa, and Yutaka Okumura: Functional complementation in mouse — human radiation hybrids assigns the putative murine scid gene to the pericentric region of human chromosome 8
Hum. Mol. Genet. 1993 2: 1031-1034; doi:10.1093/hmg/2.7.1031 [Abstract] [PDF] [Request Permissions]

SHORT REPORTS:

M.J. Hobart, B.A. Fernie, R.G. DiSciplo, and P.J. Lachmann: A physical map of the C6 and C7 complement component gene region on chromosome 5p13
Hum. Mol. Genet. 1993 2: 1035-1036; doi:10.1093/hmg/2.7.1035 [PDF] [Request Permissions]

Noboru Yokotani, Katsuml Doi, Robert J.Wenthold, and Kelji Wada: Non-conservation of a catalytic residue in a dipeptidyl aminopeptidase IV-related protein encoded by a gene on human chromosome 7
Hum. Mol. Genet. 1993 2: 1037-1039; doi:10.1093/hmg/2.7.1037 [PDF] [Request Permissions]

Jean-Marc Lobaccaro, Serge Lumbroso, Rafiaa Ktari, Robert Dumas, and Charles Sultan: An exonic point mutation creates a MaeIll site in the androgen receptor gene of a family with complete androgen insensitivity syndrome
Hum. Mol. Genet. 1993 2: 1041-1043; doi:10.1093/hmg/2.7.1041 [PDF] [Request Permissions]

MUTUAL REPORTS:

Janet Johnston, Lena Lillus, Karin Axelman, Richard Cowburn, Kurt Johansson, Matti Vlltanen, Bengt Winblad, and Lars Lannfelt: Sequencing of exons 16 and 17 of the ß-amyloid precursor protein gene fails to identify new mutations in Swedish Alzheimer's disease patients
Hum. Mol. Genet. 1993 2: 1045-1046; doi:10.1093/hmg/2.7.1045 [PDF] [Request Permissions]

Yuanhong Ma, Ming-Sun Liu, Hanfang Zhang, Ian J.Forsythe, John D.Brunzell, and Michael R.Hayden: A 4 basepair deletion in exon 4 of the human lipoprotein lipase gene results in type I hyperlipoproteinemia
Hum. Mol. Genet. 1993 2: 1049-1050; doi:10.1093/hmg/2.7.1049 [PDF] [Request Permissions]

MUTATION REPORTS:

William S.Oetting, James P.Fryer, and Richard A.King: A dinucleotide deletion (– ${Delta}$ GA115) in the tyrosinase gene responsible for type I-A (tyrosinase negative) oculocutaneous albinism in a Pakistani individual
Hum. Mol. Genet. 1993 2: 1047-1048; doi:10.1093/hmg/2.7.1047 [PDF] [Request Permissions]

Joanna P. Davies, Bryan G. Winchester, and Sue Malcolm: Mutation analysis in patients with the typical form of Anderson — Fabry disease
Hum. Mol. Genet. 1993 2: 1051-1053; doi:10.1093/hmg/2.7.1051 [PDF] [Request Permissions]

G. Marchetti, M. Ferrati, P. Patracchini, R. Redaelli, and F. Bernardi: A missense mutation (¹⁷⁸Cys ${uparrow}$ Tyr) and two neutral dimorphisms (¹¹⁵His and ³³³Ser) in the human coagulation factor VII gene
Hum. Mol. Genet. 1993 2: 1055-1056; doi:10.1093/hmg/2.7.1055 [PDF] [Request Permissions]

F. Anglani, A. Murgla, S. Bedln, E. Bresin, F. Bernardl, M. Clementi, and R. Tenconi: A new disease-causing mutation in the GAP-related domain of the NF1 gene
Hum. Mol. Genet. 1993 2: 1057-1059; doi:10.1093/hmg/2.7.1057 [PDF] [Request Permissions]

Per Guldberg, Hans C.Lou, Karen Frils Henriksen, Ingrld Mlkkelsen, Blrgltte Olsen, Birgit Hoick, and Flemmlng Guttler: A novel missense mutation in the phenylalanine hydroxylase gene of a homozygous Pakistani patient with non-PKU hyperphenylalaninemia
Hum. Mol. Genet. 1993 2: 1061-1062; doi:10.1093/hmg/2.7.1061 [PDF] [Request Permissions]

Sandra Goldenfum, Sue Malcolm, and Bryan Winchester: An 8-bp deletion in exon B of the iduronate-2-sulphatase gene in a case of Hunter disease
Hum. Mol. Genet. 1993 2: 1063-1065; doi:10.1093/hmg/2.7.1063 [PDF] [Request Permissions]

Jeremy P. Cheadle, Layla N. Al-Jader, and Allson L. Meredith: A novel nonsense mutation, W846XI (amber termination), in exon 14a of the cystic fibrosis transmembrane conductance regulator (CFTR) gene
Hum. Mol. Genet. 1993 2: 1067-1068; doi:10.1093/hmg/2.7.1067 [PDF] [Request Permissions]

Yoshitsugu Nakahashi, Hiroaki Miyazaki, Yoichi Kadota, Yuji Naitoh, Kyoichi Inoue, Masayuki Yamamoto, Norio Hayashi, and Shigeru Taketani: Human erythropoietic protoporphyria: identification of a mutation at the splice donor site of intron 7 causing exon 7 skipping of the ferrochelatase gene
Hum. Mol. Genet. 1993 2: 1069-1070; doi:10.1093/hmg/2.7.1069 [PDF] [Request Permissions]

F. Chevalier-Porst, M. Mathieu, and D. Bozon: Identification of three rare frameshift mutations in exon 13 of the cystic fibrosis gene: 1918delGC, 2118del4 and 2372del8
Hum. Mol. Genet. 1993 2: 1071-1072; doi:10.1093/hmg/2.7.1071 [PDF] [Request Permissions]

Yutaka Igarashi, Masamichi Ogawa, Takashi Kamijo, Noritaka Iwatani, Yoshikazu Nishi, Hitoshi Kohno, Takehiro Masumura, and Junichi Koga: A new mutation causing inherited growth hormone deficiency: a compound heterozygote of a 6.7 kb deletion and a two base deletion in the third exon of the GH-1 gene
Hum. Mol. Genet. 1993 2: 1073-1074; doi:10.1093/hmg/2.7.1073 [PDF] [Request Permissions]

N. Carrere, R.M. Leblanc, J. Begueret, P. Blouin, and A. Cheyrou: A new mutation of exon 5 of the P53 gene in breast cancer
Hum. Mol. Genet. 1993 2: 1075; doi:10.1093/hmg/2.7.1075 [PDF] [Request Permissions]

DNA MARKERS AND POLYMORPHISMS:

Danilo A. Tagle, Kristina L. Blanchard-McQuate, John Valdes, Lucio Castilla, and Francis S. Collins: Dinucleotide repeat polymorphisms at the D4S126 and D4S114 loci
Hum. Mol. Genet. 1993 2: 1077; doi:10.1093/hmg/2.7.1077 [PDF] [Request Permissions]

Hee-Kyung Hong, Roberto Giorda, Massimo Trucco, and Aravinda Chakravarti: Dinucleotide repeat polymorphism at the DXS1146 locus
Hum. Mol. Genet. 1993 2: 1078; doi:10.1093/hmg/2.7.1078 [PDF] [Request Permissions]

Leon Cariock and Trieu Vo: The detection of a VNTR at the Huntington disease genetic marker D4S10
Hum. Mol. Genet. 1993 2: 1079; doi:10.1093/hmg/2.7.1079 [PDF] [Request Permissions]

G.F. Sensabaugh and K.Ayer Lazaruk: A Taql site identifies the ^*A allele at the ACP1 locus
Hum. Mol. Genet. 1993 2: 1079; doi:10.1093/hmg/2.7.1079-a [PDF] [Request Permissions]

Wendy L. Flejter, Jolanta F. Kukowska-Latallo, Sam Kiousis, Settara C. Chandrasekharappa, Stephanie E. King, and Jeffrey S. Chamberlain: Tetranucleotide repeat polymorphism at D17S846 maps within 40 kb of GAS at 17q12–q22
Hum. Mol. Genet. 1993 2: 1080; doi:10.1093/hmg/2.7.1080 [PDF] [Request Permissions]

Yuan Ding, Danielle R. Reed, and R.Arlen Price: Human Bg/ll/Bc/l RFLP recognized by 3' region of human MAP 2 gene probe
Hum. Mol. Genet. 1993 2: 1080; doi:10.1093/hmg/2.7.1080-a [PDF] [Request Permissions]

H. Dollfus, J. -M. Rozet, M. A. Musarella, J. Kaplan, and A. Munnich: Dinucleotide repeat polymorphism at the human recoverin RCVI gene locus on chromosome 17p
Hum. Mol. Genet. 1993 2: 1081; doi:10.1093/hmg/2.7.1081 [PDF] [Request Permissions]

Hong Xiao, Susan E. lde, Carl R. Merril, and Mihael H. Polymeropoulos: Dinucleotide repeat polymorphism at the D11S982E locus
Hum. Mol. Genet. 1993 2: 1081; doi:10.1093/hmg/2.7.1081-a [PDF] [Request Permissions]

Patricia K. Powers and James E. Hixson: Banl and Pvull polymorphisms in intron 2 of selection E (SELE)
Hum. Mol. Genet. 1993 2: 1082; doi:10.1093/hmg/2.7.1082 [PDF] [Request Permissions]

Ludmila Saksova, Hans-Christian Hennies, and André Reis: Dinucleotide repeat polymorphism at the locus D13S231
Hum. Mol. Genet. 1993 2: 1082; doi:10.1093/hmg/2.7.1082-a [PDF] [Request Permissions]

Peter M. Brett, Georg Melmer, Mary M. Robertson, and Hugh M.D. Gurling: A microsatellite polymorphism at the THRB locus
Hum. Mol. Genet. 1993 2: 1083; doi:10.1093/hmg/2.7.1083 [PDF] [Request Permissions]

Lone B. Andersen, Susan A. Tarlé, Douglas A. Marchuk, Eric Legius, and Francis S. Collins: A compound nucleotide repeat in the neurofibro-matosis (NF1) gene
Hum. Mol. Genet. 1993 2: 1083; doi:10.1093/hmg/2.7.1083-a [PDF] [Request Permissions]

Debbi J. Birn, Timothy W. McKeithan, and Giuseppina Nucifora: An EcoRI polymorphism in the AML1 gene
Hum. Mol. Genet. 1993 2: 1084; doi:10.1093/hmg/2.7.1084 [PDF] [Request Permissions]

H.C. Watkins, C.A. MacRae, L. Thierfelder, W.J. McKenna, C.E. Seidman, and J.G. Seidman: A dinucleotide repeat polymorphism in the human LAMB2 gene on chromosome 1q
Hum. Mol. Genet. 1993 2: 1084; doi:10.1093/hmg/2.7.1084-a [PDF] [Request Permissions]

M.S. Kansara and R.S. Athwal: Dinucleotide repeat polymorphism at the D6S348 locus
Hum. Mol. Genet. 1993 2: 1085; doi:10.1093/hmg/2.7.1085 [PDF] [Request Permissions]

Barbara C. Byth and Diane W. Cox: Two consecutive dinucleotide repeats constitute an informative marker at the ${alpha}$ ₁-antichymotrypsin (AACT) locus
Hum. Mol. Genet. 1993 2: 1085; doi:10.1093/hmg/2.7.1085-a [PDF] [Request Permissions]

M.L. Delbridge and J.A. Savige: A Pstl polymorphism in the 3' end of the human type IV collagen alpha 3 chain (COL4A3) gene
Hum. Mol. Genet. 1993 2: 1086; doi:10.1093/hmg/2.7.1086 [PDF] [Request Permissions]

David F. Barker, Kim Nguyen, and Pamela R. Fain: A CA dinucleotide polymorphism at D17S107 (17q12–q24)
Hum. Mol. Genet. 1993 2: 1086; doi:10.1093/hmg/2.7.1086-a [PDF] [Request Permissions]

Kenneth Ward, Robyn Riley, Jun Lu, Margaret Robertson, and Lesa Nelson: Tetranucleotide repeat polymorphism at the D8S344 locus
Hum. Mol. Genet. 1993 2: 1087; doi:10.1093/hmg/2.7.1087 [PDF] [Request Permissions]

Michael D.Briggs and Daniel H.Cohn: Length polymorphism within a complex dinucleotide repeat in the human decorin (DCN) gene
Hum. Mol. Genet. 1993 2: 1087; doi:10.1093/hmg/2.7.1087-a [PDF] [Request Permissions]

NEW HUMAN DNA POLYMORPHISMS:

: New human DNA polymorphisms submitted to the genome data base
Hum. Mol. Genet. 1993 2: 1089-1093; doi:10.1093/hmg/2.7.1089 [PDF] [Request Permissions]

: Author index
Hum. Mol. Genet. 1993 2: 1095-1096; doi:10.1093/hmg/2.7.1095 [PDF] [Request Permissions]