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Human Molecular Genetics|July 1, 1996
Mapping of DFNB12, a gene for a non-syndromal autosomal recessive deafness, to chromosome 10q21-22H Chaib, C Place, N Salem, et al.Human Molecular Genetics|January 1, 1996
A gene responsible for a sensorineural nonsyndromic recessive deafness maps to chromosome 2p22-23H Chaïb, C Place, N Salem, et al.Human Molecular Genetics|December 1, 1993
A linkage map of human chromosome 15 with an average resolution of 2 cM and containing 55 polymorphic microsatellitesJ S Beckmann, J Tomfohrde, R I Barnes, et al.Clinical Genetics|October 12, 1999
Aicardi-Goutières syndrome: monogenic recessive disease, genetically heterogeneous disease, or multifactorial disease?S Fauré, I Bordelais, C Marquette, et al.Nature|October 24, 1985
Pseudoautosomal DNA sequences in the pairing region of the human sex chromosomesM C Simmler, F Rouyer, G Vergnaud, et al.Oncogene|May 26, 1999
Identification of three distinct regions of allelic deletions on the short arm of chromosome 8 in hepatocellular carcinomaP Pineau, H Nagai, S Prigent, et al.Cancer Letters|September 25, 1995
Precise mapping of t(12;14) leiomyoma breakpoint on chromosome 14 between D14S298 and D14S540M K Doney, S C Gerken, R Lynch, et al.Genomics|June 10, 1995
A radiation hybrid map of 95 STSs spanning human chromosome 13qS H Shaw, J E Farr, B A Thiel, et al.Human Genetics|December 1, 1995
No evidence of genetic heterogeneity in Crouzon craniofacial dysostosisH W Ma, E Lajeunie, M Le Merrer, et al.American Journal of Human Genetics|January 1, 1995
The gene for spinal cerebellar ataxia 3 (SCA3) is located in a region of approximately 3 cM on chromosome 14q24.3-q32.2G Stevanin, G Cancel, A Dürr, et al.Pageof 46