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Human Genetics|December 22, 1999
Structure of the human Lanosterol synthase gene and its analysis as a candidate for holoprosencephaly (HPE1)E Roessler, L Mittaz, Y Du, et al.Nature Genetics|November 1, 1994
A common mutation in the fibroblast growth factor receptor 1 gene in Pfeiffer syndromeM Muenke, U Schell, A Hehr, et al.American Journal of Medical Genetics|August 26, 1998
Phenotype of the fibroblast growth factor receptor 2 Ser351Cys mutation: Pfeiffer syndrome type IIIK W Gripp, C A Stolle, D M McDonald-McGinn, et al.Neuroscience|October 16, 2002
Type I bone morphogenetic protein receptors are expressed on cerebellar granular neurons and a constitutively active form of the type IA receptor induces cerebellar abnormalitiesJ E Ming, M Elkan, K Tang, et al.Nature Genetics|June 16, 1999
Mutations in the homeodomain of the human SIX3 gene cause holoprosencephalyD E Wallis, E Roessler, U Hehr, et al.Genomics|January 1, 1993
The topographic organization of repetitive DNA in the human nucleolusF S Kaplan, J Murray, J E Sylvester, et al.Molecular Psychiatry|April 20, 2004
Pedigree disequilibrium test (PDT) replicates association and linkage between DRD4 and ADHD in multigenerational and extended pedigrees from a genetic isolateM Arcos-Burgos, F X Castellanos, D Konecki, et al.American Journal of Human Genetics|May 1, 1993
Molecular analysis of the 18q- syndrome--and correlation with phenotypeA D Kline, M E White, R Wapner, et al.The Journal of Molecular and Cellular Immunology : JMCI|January 1, 1989
Interleukin 6 is the principal cytolytic T lymphocyte differentiation factor for thymocytes in human leukocyte conditioned mediumJ E Ming, C Cernetti, R M Steinman, et al.Proceedings of the National Academy of Sciences of the United States of America|August 16, 1994
Linkage of a human brain malformation, familial holoprosencephaly, to chromosome 7 and evidence for genetic heterogeneityM Muenke, F Gurrieri, C Bay, et al.Pageof 12