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American Journal of Medical Genetics|January 1, 1983
Brief clinical report: ring-11 chromosome: phenotype-karyotype correlation with deletions of 11qA J Cousineau, J V Higgins, A B Scott-Emuakpor, et al.American Journal of Medical Genetics|January 1, 1980
Discriminating among single locus models using small pedigreesT H BeatyAmerican Journal of Medical Genetics|September 1, 1982
Spondylohumerofemoral hypoplasia (giant cell chondrodysplasia): a neonatally lethal short-limbed skeletal displasiaD O Sillence, R S Lachman, T Jenkins, et al.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|January 1, 1984
An anthropometric study of males with the fragile-X syndromeD L Meryash, C E Cronk, B Sachs, et al.American Journal of Medical Genetics|January 1, 1984
A form of X-linked mental retardation with marfanoid habitusJ E Lujan, M E Carlin, H A LubsAmerican Journal of Medical Genetics|March 1, 1984
Brief clinical report: Curry-Hall syndromeS D Shapiro, R J Jorgenson, C F SalinasAmerican Journal of Medical Genetics|March 1, 1984
Incontinentia pigmenti in a father and his daughterA Sommer, P H LiuAmerican Journal of Medical Genetics|February 1, 1984
Ring chromosome 14 and immunoglobulin locusM Krawczun, G Melink, J CervenkaAmerican Journal of Medical Genetics|December 1, 1983
A previously undescribed autosomal recessive multiple congenital anomalies/mental retardation (MCA/MR) syndrome with growth failure, lip/palate cleft(s), and urogenital anomaliesG Malpuech, F Demeocq, J B Palcoux, et al.Pageof 854