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Nature Genetics|September 1, 1995
Dominant mutations in the type II collagen gene, COL2A1, produce spondyloepimetaphyseal dysplasia, Strudwick typeG E Tiller, P A Polumbo, M A Weis, et al.American Journal of Medical Genetics|September 13, 2000
Cole-Hughes macrocephaly syndrome and associated autistic manifestationsS Naqvi, T Cole, J M GrahamAnalytical Biochemistry|June 1, 1990
Isolation of the major subcellular organelles from mouse liver using Nycodenz gradients without the use of an ultracentrifugeJ M Graham, T Ford, D RickwoodAmerican Journal of Medical Genetics|April 1, 1984
Syndrome of multiple pterygia, camptodactyly, facial anomalies, hypoplastic lungs and heart, cystic hygroma, and skeletal anomalies: delineation of a new entity and review of lethal forms of multiple pterygium syndromeH Chen, L Immken, R Lachman, et al.The Journal of Biological Chemistry|March 21, 1998
Structurally abnormal type II collagen in a severe form of Kniest dysplasia caused by an exon 24 skipping mutationM A Weis, D J Wilkin, H J Kim, et al.American Journal of Medical Genetics|July 1, 1990
Possible heterogeneity in spondyloenchondrodysplasia: quadriparesis, basal ganglia calcifications, and chondrocyte inclusionsM Frydman, J Bar-Ziv, R Preminger-Shapiro, et al.American Journal of Medical Genetics|October 1, 1984
Fibrochondrogenesis: radiologic and histologic studiesD J Eteson, G E Adomian, A Ornoy, et al.Obstetrics and Gynecology|January 11, 1976
The clinical syndrome of triploidyW Wertelecki, J M Graham, F R SergovichClinical Pediatrics|May 18, 1999
Williams-Beuren syndrome: an update and review for the primary physicianA Lashkari, A K Smith, J M GrahamPediatrics|June 1, 1981
Central nervous system and facial defects associated with maternal hyperthermia at four to 14 weeks' gestationH Pleet, J M Graham, D W SmithPageof 42