Showing results (171-180 of 6,483) with videos related to
Sort By:
Pageof 649
Journal of Medical Genetics|January 1, 1992
Familial Scheuermann disease: a genetic and linkage studyL McKenzie, D SillenceJournal of Medical Genetics|January 1, 1992
Estimation of the size of the chromosome 17p11.2 duplication in Charcot-Marie-Tooth neuropathy type 1a (CMT1a). HMSN Collaborative Research GroupP Raeymaekers, V Timmerman, E Nelis, et al.Journal of Medical Genetics|November 3, 2004
Sequence family variant loss from the AZFc interval of the human Y chromosome, but not gene copy loss, is strongly associated with male infertilityN Machev, N Saut, G Longepied, et al.Journal of Medical Genetics|November 3, 2004
FRG2, an FSHD candidate gene, is transcriptionally upregulated in differentiating primary myoblast cultures of FSHD patientsT Rijkers, G Deidda, S van Koningsbruggen, et al.Journal of Medical Genetics|June 17, 2005
A novel locus for autosomal dominant non-syndromic deafness, DFNA53, maps to chromosome 14q11.2-q12D Yan, X Ke, S H Blanton, et al.Journal of Medical Genetics|June 7, 2005
Comprehensive analysis of CDKN2A (p16INK4A/p14ARF) and CDKN2B genes in 53 melanoma index cases considered to be at heightened risk of melanomaK Laud, C Marian, M F Avril, et al.Journal of Medical Genetics|June 7, 2005
Identification of predicted human outer dynein arm genes: candidates for primary ciliary dyskinesia genesG J Pazour, N Agrin, B L Walker, et al.Journal of Medical Genetics|June 7, 2005
TNFalpha and IL10 SNPs act together to predict disease behaviour in Crohn's diseaseE V Fowler, R Eri, G Hume, et al.Journal of Medical Genetics|August 25, 2005
Confirmation of CHD7 as a cause of CHARGE association identified by mapping a balanced chromosome translocation in affected monozygotic twinsD Johnson, N Morrison, L Grant, et al.Pageof 649