Showing results (51-60 of 103) with videos related to
Sort By:
Pageof 11
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.Journal of Medical Genetics|September 11, 1998
Familial craniosynostosis, anal anomalies, and porokeratosis: CAP syndromeN Flanagan, S A Boyadjiev, J Harper, 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.Genomics|February 1, 1994
A YAC contig of approximately 3 Mb from human chromosome 5q31-->q33X Li, C A Wise, D Le Paslier, et al.American Journal of Medical Genetics. Part A|January 28, 2003
Facial dysgenesis: a novel facial syndrome with chromosome 7 deletion p15.1-21.1Julie E Hoover-Fong, J Cai, C B Cargile, et al.American Journal of Medical Genetics|July 16, 1999
Ocular anterior chamber dysgenesis in craniosynostosis syndromes with a fibroblast growth factor receptor 2 mutationK Okajima, L K Robinson, M A Hart, et al.Proceedings of the National Academy of Sciences of the United States of America|April 1, 1997
TCOF1 gene encodes a putative nucleolar phosphoprotein that exhibits mutations in Treacher Collins Syndrome throughout its coding regionC A Wise, L C Chiang, W A Paznekas, et al.Cytogenetics and Cell Genetics|January 1, 1995
Localization of the human stem cell tyrosine kinase-1 gene (FLT3) to 13q12-->q13C E Carow, E Kim, A L Hawkins, et al.Pageof 11