Hum. Mol. Genet. -- Table of Contents (1 [8] )

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Contents: Volume 1, Number 8   October 1992   [Index by Author]

       ORIGINAL ARTICLES

       SHORT REPORT

       MUTATION REPORTS

       HUMAN DNA POLYMORPHISMS

       Author index

       Corrigendum

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ORIGINAL ARTICLES:

Shuichi Nakatsuru, Akio Yanagisawa, Shigetoshi Ichii, Eiichi Tahara, Yo Kato, Yusuke Nakamura, and Akira Horii: Somatic mutation of the APC gene in gastric cancer: frequent mutations in very well differentiated adenocarcinoma and signet-ring cell carcinoma
Hum. Mol. Genet. 1992 1: 559-563; doi:10.1093/hmg/1.8.559 [Abstract] [PDF] [Request Permissions]

Marianne Antoine and Mike Fried: The organization of the intron-containing human S6 ribosomal protein (rpS6) gene and determination of its location at chromosome 9p21
Hum. Mol. Genet. 1992 1: 565-570; doi:10.1093/hmg/1.8.565 [Abstract] [PDF] [Request Permissions]

R.Scott Hansen, Stanley M. Gartler, C.Ronald Scott, Shi-Han Chen, and Charles M. xLaird: Methylation analysis of CGG sites in the CpG island of the human FMR1 gene
Hum. Mol. Genet. 1992 1: 571-578; doi:10.1093/hmg/1.8.571 [Abstract] [PDF] [Request Permissions]

Ann P. Walker, Jamel Chelly, Donald R. Love, Yumiko Ishikawa Brush, Dominique Récan, Jean-Louis Chaussain, Christine A. Oley, J.Michael Connor, John Yates, David A. Price, Maurice Super, Armand Bottani, Beat Steinman, Jean-Claude Kaplan, Kay E. Davies, and Anthony P. Monaco: A YAC contig in Xp21 containing the adrenal hypoplasia congenita and glycerol kinase deficiency genes
Hum. Mol. Genet. 1992 1: 579-585; doi:10.1093/hmg/1.8.579 [Abstract] [PDF] [Request Permissions]

J. Wiegant, W. Kalle, L. Mullenders, S. Brookes, J.M.N. Hoovers, J.G. Dauwerse, G.J.B. van Ommen, and A.K. Raap: High-resolution in situ hybridization using DNA halo preparations
Hum. Mol. Genet. 1992 1: 587-591; doi:10.1093/hmg/1.8.587 [Abstract] [PDF] [Request Permissions]

J.G. Dauwerse, J. Wiegant, A.K. Raap, M.H. Breuning, and G.J.B. van Ommen: Multiple colors by fluorescence in situ hybridization using ratio-labelled DNA probes create a molecular karyotype
Hum. Mol. Genet. 1992 1: 593-598; doi:10.1093/hmg/1.8.593 [Abstract] [PDF] [Request Permissions]

Claudine Oudet, André Hanauer, Paula Clemens, Thomas Caskey, and Jean-Louis Mandel: Two hot spots of recombination in the DMD gene correlate with the deletion prone regions
Hum. Mol. Genet. 1992 1: 599-603; doi:10.1093/hmg/1.8.599 [Abstract] [PDF] [Request Permissions]

B.W. Nieuwenhuijsen, K.L. Chen, A.C. Chinault, S. Wang, V.H. Valmiki, E.J. Meershoek, G.J.B. van Ommen, and V.H. Fischbeck: A yeast artificial chromosome contig spanning the Charcot — Marie — Tooth disease type 1A duplication region
Hum. Mol. Genet. 1992 1: 605-612; doi:10.1093/hmg/1.8.605 [Abstract] [PDF] [Request Permissions]

Rebecca J. Oakey, Mark L. Watson, and Michael F. Seldin: Construction of a physical map on mouse and human chromosome 1: comparison of 13 Mb of mouse and 11 Mb of human DNA
Hum. Mol. Genet. 1992 1: 613-620; doi:10.1093/hmg/1.8.613 [Abstract] [PDF] [Request Permissions]

Isabelle Richard, Odile Broux, Dominique Hillaire, Dorra Cherif, Françoise Fougerousse, Daniel Cohen, and Jacques S. Beckmann: Mapping of the formin gene and exclusion as a candidate gene for the autosomal recessive form of limb-girdle muscular dystrophy
Hum. Mol. Genet. 1992 1: 621-624; doi:10.1093/hmg/1.8.621 [Abstract] [PDF] [Request Permissions]

Stefan Joos, Martin H. Falk, Peter Lichter, Frank G. Haluska, Berthold Henglein, Gilbert M. Lenoir, and Georg W. Bornkamm: Variable breakpoints in Burkitt lymphoma cells with chromosomal t(8; 14) translocation separate c-myc and the IgH locus up to several hundred kb
Hum. Mol. Genet. 1992 1: 625-632; doi:10.1093/hmg/1.8.625 [Abstract] [PDF] [Request Permissions]

Jennifer C. Knight, Brian R. Reeves, Lyndal Kearney, Anthony P. Monaco, Hans Lehrach, and Colin S. Cooper: Localization of the synovial sarcoma t(X;18)(p11.2;q11.2) breakpoint by fluorescence in situ hybridization
Hum. Mol. Genet. 1992 1: 633-637; doi:10.1093/hmg/1.8.633 [Abstract] [PDF] [Request Permissions]

SHORT REPORT:

Timothy C. Cox, Helen M. Kozman, Wendy H. Raskind, Brian K. May, and John C. Mulley: Identification of a highly polymorphic marker within intron 7 of the ALAS2 gene and suggestion of at least two loci for X-linked sideroblastic anemia
Hum. Mol. Genet. 1992 1: 639-641; doi:10.1093/hmg/1.8.639 [Abstract] [PDF] [Request Permissions]

MUTATION REPORTS:

Yohsuke Minatogawa, Shigenobu Tone, Jennifer Allsop, P.Edward Purdue, Yoshikazu Takada, Christopher J. Danpur, and Ryo Kido: A serine-to-phenylalanine substitution leads to loss of alanine: glyoxylate aminotransferase catalytic activity and immunoreactivity in a patient with primary hyperoxaluria type 1
Hum. Mol. Genet. 1992 1: 643-644; doi:10.1093/hmg/1.8.643 [PDF] [Request Permissions]

A.V. Winnard, Y. Jia-Hsu, R.A. Gibbs, J.R. Mendell, and A.H.M. Burghes: Identification of a 2 base pair nonsense mutation causing a cryptic splice site in a DMD patient
Hum. Mol. Genet. 1992 1: 645-646; doi:10.1093/hmg/1.8.645 [PDF] [Request Permissions]

F. Chevalier-Porst, J.C. Chomel, D. Hillaire, A. Kitzis, J.C. Kaplan, R. Goutaland, M. Mathieu, and D. Bozon: A nonsense mutation in exon 4 of the cystic fibrosis gene frequent among the population of the Reunion Island
Hum. Mol. Genet. 1992 1: 647-648; doi:10.1093/hmg/1.8.647 [PDF] [Request Permissions]

Thilo Papp, Mehrdad Jafari, Corinna Kopp, and Dietmar Schiffmann: Acil and BstNI/Cfrl detect all possible activating point mutations at codons 13 and 61 of the human H-ras oncogene
Hum. Mol. Genet. 1992 1: 649; doi:10.1093/hmg/1.8.649 [PDF] [Request Permissions]

HUMAN DNA POLYMORPHISMS:

D.H. Donaldson, D.R. Rosen, J. O'Regan, P.C. Sapp, H.R. Horvitz, J.F. Gusella, J.L. Haines, S. Pestka, V. Jung, C. Nusbaum, D. Patterson, and R.H. Brown, Jr: Two independent dinucleotide repeat polymorphisms at the D21S235 locus (21q22.1)
Hum. Mol. Genet. 1992 1: 651; doi:10.1093/hmg/1.8.651 [PDF] [Request Permissions]

Hong Xiao, Carl R. Merril, and Mihael H. Polymeropoulos: Dinucleotide repeat polymorphisms at the D3S1246 and D3S1247 loci
Hum. Mol. Genet. 1992 1: 652; doi:10.1093/hmg/1.8.652 [PDF] [Request Permissions]

M. de Weers, R.G.J. Mensink, M. Kenter, and R.K.B. Schuurman: Three dinucleotide repeat polymorphisms at the DXS178 locus
Hum. Mol. Genet. 1992 1: 653; doi:10.1093/hmg/1.8.653 [PDF] [Request Permissions]

J. Gärtner, C. Obie, H. Moser, and D. Valle: A polymorphic synonymous mutation (K54K) in the human 70 kD peroxisomal membrane protein gene (PMP1)
Hum. Mol. Genet. 1992 1: 654; doi:10.1093/hmg/1.8.654 [PDF] [Request Permissions]

David J. Koorey, Geoffrey W. McCaughan, Ronald J. Trent, and Neil D. Gallagher: Dinucleotide repeat polymorphism at the D5S134 locus linked to the adenomatous polyposis coli (APC) gene
Hum. Mol. Genet. 1992 1: 655; doi:10.1093/hmg/1.8.655 [PDF] [Request Permissions]

Yuan Ding, Danielle R. Reed, John P. Vuchetich, and R. Arlen Price: Human Bg/II/Bc/I RFLP recognized by 5' region of human MAP 2 gene probe
Hum. Mol. Genet. 1992 1: 655; doi:10.1093/hmg/1.8.655-a [PDF] [Request Permissions]

M. Stoffel, K. Xiang, and G.I. Bell: Dinucleotide repeat polymorphism at the human ribophorin II locus (RPN2) on chromosome 20q
Hum. Mol. Genet. 1992 1: 656; doi:10.1093/hmg/1.8.656 [PDF] [Request Permissions]

L. Pulik, K.J. Gratton, and N.T. Bech-Hansen: Taql RFLP in the region of the human homeobox PBX3 gene
Hum. Mol. Genet. 1992 1: 656; doi:10.1093/hmg/1.8.656-a [PDF] [Request Permissions]

E.I. Rogaev and S.A. Keryanov: Unusual variability of the complex dinucleotide repeat block at the SPN locus
Hum. Mol. Genet. 1992 1: 657; doi:10.1093/hmg/1.8.657 [PDF] [Request Permissions]

John I. Risinger and Jeff Boyd: Dinucleotide repeat polymorphism in the human DCC gene at chromosome 18q21
Hum. Mol. Genet. 1992 1: 657; doi:10.1093/hmg/1.8.657-a [PDF] [Request Permissions]

Mihael H. Polymeropoulos, Hong Xiao, and Carl R. Merril: Tetranucleotide repeat polymorphism at the human myelin basic protein gene (MBP)
Hum. Mol. Genet. 1992 1: 658; doi:10.1093/hmg/1.8.658 [PDF] [Request Permissions]

David J. Kwiatkowski and Manuel O. Diaz: Dinucleotide repeat polymorphism at the IFNA locus (9p22)
Hum. Mol. Genet. 1992 1: 658; doi:10.1093/hmg/1.8.658-a [PDF] [Request Permissions]

Ronald G. Gregg and Molly B. Parker: Dinucleotide repeat polymorphism at the D7S547 locus
Hum. Mol. Genet. 1992 1: 659; doi:10.1093/hmg/1.8.659 [PDF] [Request Permissions]

W.H.I. McLean and E.B. Lane: Avall RFLP of human keratin 10 (KRT-10) detected by PCR
Hum. Mol. Genet. 1992 1: 659; doi:10.1093/hmg/1.8.659-a [PDF] [Request Permissions]

E. Martínez-Cáceres, M. Juan, M. Romero, I. Rojo, and J. Martorell: Rsal polymorphism of the human CD27 gene, a member of nerve growth factor receptor gene family
Hum. Mol. Genet. 1992 1: 660; doi:10.1093/hmg/1.8.660 [PDF] [Request Permissions]

Author index:

: Author index
Hum. Mol. Genet. 1992 1: 661; doi:10.1093/hmg/1.8.661 [PDF] [Request Permissions]

Corrigendum:

R.W. Hendriks, Z.-Y. Chen, H. Hinds, R.K.B. Schuurman, and I.W. Craig: An X chromosome inactivation assay based on differential methylation of a CpG island coupled to a VNTR polymorphism at the 5' end of the Monoamine Oxidase A gene
Hum. Mol. Genet. 1992 1: 662; doi:10.1093/hmg/1.8.662 [Abstract] [PDF] [Request Permissions]

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