Showing results (451-460 of 11,953) with videos related to
Sort By:
Pageof 1,196
Human Molecular Genetics|December 1, 1996
Ataxia-telangiectasia: founder effect among north African JewsS Gilad, A Bar-Shira, R Harnik, et al.Human Molecular Genetics|January 1, 1996
In vivo amplification of the PAX3-FKHR and PAX7-FKHR fusion genes in alveolar rhabdomyosarcomaF G Barr, L E Nauta, R J Davis, et al.Human Molecular Genetics|January 1, 1996
Cloning and characterization of a murine brain specific gene Bpx and its human homologue lying within the Xic candidate regionC Rougeulle, P AvnerHuman Molecular Genetics|January 1, 1996
An animal model for Norrie disease (ND): gene targeting of the mouse ND geneW Berger, D van de Pol, D Bächner, et al.Human Molecular Genetics|January 1, 1996
Developmental expression of the Fac gene correlates with congenital defects in Fanconi anemia patientsF Krasnoshtein, M BuchwaldHuman Molecular Genetics|January 1, 1996
Autosomal recessive non-syndromic deafness locus (DFNB8) maps on chromosome 21q22 in a large consanguineous kindred from PakistanA Veske, R Oehlmann, F Younus, et al.Human Molecular Genetics|January 1, 1996
Linkage studies of non-syndromic recessive deafness (NSRD) in a family originating from the Mirpur region of Pakistan maps DFNB1 centromeric to D13S175K A Brown, A H Janjua, G Karbani, et al.Human Molecular Genetics|November 13, 1998
Multilocus linkage identifies two new loci for a mendelian form of stroke, cerebral cavernous malformation, at 7p15-13 and 3q25.2-27H D Craig, M Günel, O Cepeda, et al.Human Molecular Genetics|November 13, 1998
Analysis of the human GDNF gene reveals an inducible promoter, three exons, a triplet repeat within the 3'-UTR and alternative splice productsL Grimm, E Holinski-Feder, J Teodoridis, et al.Human Molecular Genetics|November 13, 1998
Mutations in DPC4 (SMAD4) cause juvenile polyposis syndrome, but only account for a minority of casesR Houlston, S Bevan, A Williams, et al.Pageof 1,196