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American Journal of Human Genetics|March 1, 1997
Dominant inheritance of isolated hypermethioninemia is associated with a mutation in the human methionine adenosyltransferase 1A geneM E Chamberlin, T Ubagai, S H Mudd, et al.American Journal of Human Genetics|March 1, 1997
A unique point mutation in the fibroblast growth factor receptor 3 gene (FGFR3) defines a new craniosynostosis syndromeM Muenke, K W Gripp, D M McDonald-McGinn, et al.American Journal of Human Genetics|March 1, 1997
Molecular analysis of cystinuria in Libyan Jews: exclusion of the SLC3A1 gene and mapping of a new locus on 19qR Wartenfeld, E Golomb, G Katz, et al.American Journal of Human Genetics|March 1, 1997
Hereditary spastic paraplegia: LOD-score considerations for confirmation of linkage in a heterogeneous traitM P Dubé, M A Mlodzienski, Z Kibar, et al.American Journal of Human Genetics|March 1, 1997
Anticipation or ascertainment bias in schizophrenia? Penrose's familial mental illness sampleA S Bassett, J HustedAmerican Journal of Human Genetics|March 1, 1997
Segregation analysis of cryptogenic epilepsy and an empirical test of the validity of the resultsR Ottman, W A Hauser, C Barker-Cummings, et al.American Journal of Human Genetics|March 1, 1997
Transmission-disequilibrium tests for quantitative traitsD B AllisonAmerican Journal of Human Genetics|March 1, 1997
HLA class II DR-DQ amino acids and insulin-dependent diabetes mellitus: application of the haplotype methodA M Valdes, S McWeeney, G ThomsonAmerican Journal of Human Genetics|April 1, 1997
Somatic inactivation of the VHL gene in Von Hippel-Lindau disease tumorsA H Prowse, A R Webster, F M Richards, et al.American Journal of Human Genetics|April 1, 1997
Mutational analysis of the PEX gene in patients with X-linked hypophosphatemic ricketsI A Holm, X Huang, L M KunkelPageof 979