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Neuromuscular Disorders : NMD|September 1, 1994
Linkage analyses between dominant X-linked Charcot-Marie-Tooth disease, and 15 Xq11-Xq21 microsatellites in a new large family: three new markers are closely linked to the geneE Le Guern, N Ravise, M Gugenheim, et al.
Human Genetics|August 1, 1987
Absence of Y-specific DNA sequences in human 46,XX true hermaphrodites and in 45,X mixed gonadal dysgenesisF Waibel, G Scherer, M Fraccaro, et al.
British Journal of Cancer|November 1, 1995
Loss of heterozygosity in sporadic breast tumours at the BRCA2 locus on chromosome 13q12-q13A M Cleton-Jansen, N Collins, S R Lakhani, et al.
Annals of Human Genetics|October 1, 1995
Integrated genetic map of human chromosome 2S Cox, S P Bryant, A Collins, et al.
American Journal of Human Genetics|January 1, 1995
Autosomal dominant familial spastic paraplegia: reduction of the FSP1 candidate region on chromosome 14q to 7 cM and locus heterogeneityS Gispert, N Santos, R Damen, et al.
Neurology|December 1, 1994
Hereditary neuralgic amyotrophy and hereditary neuropathy with liability to pressure palsies: two distinct clinical, electrophysiologic, and genetic entitiesR Gouider, E LeGuern, J Emile, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 1, 1980
Two interferon mRNAs in human fibroblasts: in vitro translation and Escherichia coli cloning studiesJ Weissenbach, Y Chernajovsky, M Zeevi, et al.
Human Genetics|September 16, 1998
Genetic linkage of progressive pseudorheumatoid dysplasia to a 3-cM interval of chromosome 6q22J Fischer, J A Urtizberea, S Pavek, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 1, 1993
A 4.5-megabase yeast artificial chromosome contig from human chromosome 13q14.3 ordering 9 polymorphic microsatellites (22 sequence-tagged sites) tightly linked to the Wilson disease locusA White, J Tomfohrde, E Stewart, et al.
Human Genetics|October 1, 1986
A 45,X male with a Yp/18 translocationE Maserati, F Waibel, B Weber, et al.
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