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Biochemical and Biophysical Research Communications|October 10, 1992
Structure of the human spermidine/spermine N1-acetyltransferase gene (exon/intron gene organization and localization to Xp22.1)L Xiao, P Celano, A R Mank, et al.Genomics|January 1, 1991
Alphoid DNA polymorphisms for chromosome 21 can be distinguished from those of chromosome 13 using probes homologous to bothE W Jabs, A C Warren, E W Taylor, et al.Molecular Biology of the Cell|September 12, 2000
Characterization of the nucleolar gene product, treacle, in Treacher Collins syndromeC Isaac, K L Marsh, W A Paznekas, et al.Human Genetics|January 1, 1997
Evidence for an association between markers on chromosome 19q and non-syndromic cleft lip with or without cleft palate in two groups of multiplex familiesD F Wyszynski, N Maestri, I McIntosh, et al.Genomics|July 15, 1994
Two craniosynostotic syndrome loci, Crouzon and Jackson-Weiss, map to chromosome 10q23-q26X Li, A F Lewanda, F Eluma, et al.Journal of Medical Genetics|September 11, 1998
Familial craniosynostosis, anal anomalies, and porokeratosis: CAP syndromeN Flanagan, S A Boyadjiev, J Harper, et al.Genomics|January 1, 1994
Genetic heterogeneity among craniosynostosis syndromes: mapping the Saethre-Chotzen syndrome locus between D7S513 and D7S516 and exclusion of Jackson-Weiss and Crouzon syndrome loci from 7pA F Lewanda, M M Cohen, C E Jackson, et al.Genomics|December 1, 1992
Human dopamine transporter gene (DAT1) maps to chromosome 5p15.3 and displays a VNTRD J Vandenbergh, A M Persico, A L Hawkins, et al.American Journal of Otolaryngology|January 1, 1983
Sclerosteosis involving the temporal bone: clinical and radiologic aspectsG T Nager, S A Stein, J P Dorst, et al.Human Molecular Genetics|July 1, 1995
Novel FGFR2 mutations in Crouzon and Jackson-Weiss syndromes show allelic heterogeneity and phenotypic variabilityW J Park, G A Meyers, X Li, et al.Pageof 11