Showing results (661-670 of 6,484) with videos related to
Sort By:
Pageof 649
Journal of Medical Genetics|July 1, 1992
Unknown syndrome in sibs: pili torti, growth delay, developmental delay, and mild neurological abnormalitiesS K Shapira, A S Neish, B R PoberJournal of Medical Genetics|June 1, 1992
Terminal 22q deletion associated with a partial deficiency of arylsulphatase AK Narahara, Y Takahashi, M Murakami, et al.Journal of Medical Genetics|August 1, 1992
Nine cystic fibrosis patients homozygous for the CFTR nonsense mutation R1162X have mild or moderate lung diseaseP Gasparini, G Borgo, G Mastella, et al.Journal of Medical Genetics|August 1, 1992
Linkage of epidermolysis bullosa simplex to keratin gene lociK E McKenna, A E Hughes, E A Bingham, et al.Journal of Medical Genetics|October 1, 1976
Association of D/D translocations with fetal wastage and aneuploidy. A report of four familiesP M Fernhoff, D N Singh, J Hanson, et al.Journal of Medical Genetics|October 1, 1976
A giant short arm of no. 21 chromosome in mother of 21/21 translocation mongolE Tuncbilek, M Bobrow, G Clarke, et al.Journal of Medical Genetics|September 1, 1992
Identification of a new DMD gene deletion by ectopic transcript analysisF Rininsland, A Hahn, S Niemann-Seyde, et al.Journal of Medical Genetics|November 25, 2003
Identification of recurrent regions of chromosome loss and gain in vestibular schwannomas using comparative genomic hybridisationC Warren, L A James, R T Ramsden, et al.Journal of Medical Genetics|October 22, 2003
In vivo reversion to normal of inherited mutations in humansR HirschhornJournal of Medical Genetics|October 22, 2003
Homozygosity mapping of a gene for arterial tortuosity syndrome to chromosome 20q13P J Coucke, M W Wessels, P Van Acker, et al.Pageof 649