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Archives of Ophthalmology (Chicago, Ill. : 1960)|August 1, 1983
Ocular histopathology and ultrastructure of Sanfilippo's syndrome, type III-BM A Lavery, W R Green, E W Jabs, et al.Genomics|August 29, 1998
Human SLUG gene organization, expression, and chromosome map location on 8qM E Cohen, M Yin, W A Paznekas, et al.American Journal of Medical Genetics|December 14, 1999
Clinical, cytogenetic, and fluorescence in situ hybridization findings in two cases of "complete ring" syndromeS Sigurdardottir, B K Goodman, J Rutberg, et al.Human Genetics|May 1, 1994
Chromosomal localization of genes required for the terminal steps of oxidative metabolism: alpha and gamma subunits of ATP synthase and the phosphate carrierE W Jabs, P J Thomas, M Bernstein, et al.Human Genetics|September 12, 2000
Physical mapping of the human ATX1 homologue (HAH1) to the critical region of the 5q- syndrome within 5q32, and immediately adjacent to the SPARC geneJ Boultwood, A J Strickson, E W Jabs, et al.American Journal of Human Genetics|December 18, 1997
Autosomal dominant postaxial polydactyly, nail dystrophy, and dental abnormalities map to chromosome 4p16, in the region containing the Ellis-van Creveld syndrome locusT D Howard, A E Guttmacher, W McKinnon, et al.Genomics|September 1, 1991
Mapping the Treacher Collins syndrome locus to 5q31.3----q33.3E W Jabs, X Li, C A Coss, et al.Cytogenetics and Cell Genetics|January 1, 1993
Mapping the intron-containing human hsp90 alpha (HSPCAL4) gene to chromosome band 14q32N C Vamvakopoulos, C A Griffin, A L Hawkins, et al.American Journal of Medical Genetics|May 26, 1998
Syndrome of coronal craniosynostosis with brachydactyly and carpal/tarsal coalition due to Pro250Arg mutation in FGFR3 geneJ M Graham, S R Braddock, G R Mortier, et al.Prenatal Diagnosis|December 17, 1997
Prenatal ultrasonographic and molecular diagnosis of Apert syndromeK Filkins, J F Russo, S Boehmer, et al.Pageof 11