Showing results (71-80 of 77) with videos related to
Sort By:
Pageof 8
You have reached the last page of results.This site can display upto 77 results.
American Journal of Medical Genetics|August 1, 1983
Part II. Amyoplasia: twinning in amyoplasia--a specific type of arthrogryposis with an apparent excess of discordantly affected identical twinsJ G Hall, S D Reed, B C McGillivray, et al.American Journal of Medical Genetics|February 1, 1984
Terminal and interstitial deletions of the long arm of chromosome 7: a review with five new casesR S Young, D D Weaver, M K Kukolich, et al.American Journal of Medical Genetics|April 15, 2000
Exclusion of the branchio-oto-renal syndrome locus (EYA1) from patients with branchio-oculo-facial syndromeA E Lin, E V Semina, S Daack-Hirsch, et al.Journal of Medical Genetics|August 14, 2008
Mutations in JARID1C are associated with X-linked mental retardation, short stature and hyperreflexiaF E Abidi, L Holloway, C A Moore, et al.American Journal of Medical Genetics|October 6, 1999
Mild autosomal dominant hypophosphatasia: in utero presentation in two familiesC A Moore, C J Curry, P S Henthorn, et al.American Journal of Medical Genetics|July 17, 1995
Cytogenetic and molecular analysis of a ring (21) in a patient with partial trisomy 21 and megakaryocytic leukemiaC G Palmer, J L Blouin, M J Bull, et al.Journal of Medical Genetics|April 5, 2005
Multiple mechanisms are implicated in the generation of 5q35 microdeletions in Sotos syndromeK Tatton-Brown, J Douglas, K Coleman, et al.Pageof 8