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Human Genetics|May 1, 1997
Exclusion of ZFM1 as a candidate gene for multiple endocrine neoplasia type 1 (MEN1)S E Lloyd, J T Pang, S H Pearce, et al.Human Genetics|May 1, 1997
Comparative genomic hybridization reveals a partial de novo trisomy 6q23-qter in an infant with congenital malformations: delineation of the phenotypeM Erdel, H C Duba, I Verdorfer, et al.Human Genetics|May 1, 1997
The tricho-rhino-phalangeal syndromes: frequency and parental origin of 8q deletionsJ Nardmann, L Tranebjaerg, B Horsthemke, et al.Human Genetics|May 1, 1997
Mutations and sequence variants in the testis-determining region of the Y chromosome in individuals with a 46,XY female phenotypeR Veitia, A Ion, S Barbaux, et al.Human Genetics|May 1, 1997
Refinement of the hereditary neuralgic amyotrophy (HNA) locus to chromosome 17q24-q25F Stögbauer, P Young, V Timmerman, et al.Human Genetics|October 6, 1998
Phenotypic variation in a family with mutations in two Hirschsprung-related genes (RET and endothelin receptor B)P J Svensson, M Anvret, M L Molander, et al.Human Genetics|October 6, 1998
The Usher syndrome in the Lebanese population and further refinement of the USH2A candidate regionM Saouda, A Mansour, Y Bou Moglabey, et al.Human Genetics|October 6, 1998
Variation of site-specific methylation patterns in the factor VIII (F8C) gene in human sperm DNAD S Millar, M Krawczak, D N CooperHuman Genetics|October 6, 1998
Genotype/phenotype correlation in affected individuals of a family with a deletion of the entire coding sequence of the connexin 32 geneP J Ainsworth, C F Bolton, B C Murphy, et al.Human Genetics|October 6, 1998
Molecular characterization and mutational analysis of the human B17 subunit of the mitochondrial respiratory chain complex IJ Smeitink, J Loeffen, R Smeets, et al.Pageof 957