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American Journal of Medical Genetics|January 15, 1993
Moderately severe osteogenesis imperfecta associated with substitutions of serine for glycine in the alpha 1(I) chain of type I collagenJ C Marini, M B Lewis, K ChenHolistic Nursing Practice|July 1, 1995
"He calls me his angel of mercy": the experience of caring for elderly parents in the homeM B Lewis, M P Curtis, K S LundyAmerican Journal of Medical Genetics|June 1, 1990
Analysis of cultured chorionic villi in a case of osteogenesis imperfecta type II: implications for prenatal diagnosisD K Grange, M B Lewis, J C MariniAmerican Journal of Medical Genetics|August 1, 1991
Familial holoprosencephaly associated with a translocation breakpoint at chromosomal position 7q36A G Hatziioannou, C M Krauss, M B Lewis, et al.Nucleic Acids Research|July 25, 1990
Detection of point mutations in type I collagen by RNase digestion of RNA/RNA hybridsD K Grange, G S Gottesman, M B Lewis, et al.Human Mutation|January 1, 1993
A de novo G+1-->A mutation at the alpha 2(I) exon 16 splice donor site causes skipping of exon 16 in the cDNA of one allele of an OI type IV probandJ D Filie, B M Orrison, Q Wang, et al.Neuroendocrinology|January 1, 1986
Differential production of SRIF 14 and 28 by fetal rat hypothalamic cells enriched by velocity sedimentationM D Lewis, S M Foord, M B Lewis, et al.The Journal of Biological Chemistry|February 5, 1993
Serine for glycine substitutions in type I collagen in two cases of type IV osteogenesis imperfecta (OI). Additional evidence for a regional model of OI pathophysiologyJ C Marini, M B Lewis, Q Wang, et al.The Journal of Biological Chemistry|July 15, 1989
Osteogenesis imperfecta type IV. Detection of a point mutation in one alpha 1(I) collagen allele (COL1A1) by RNA/RNA hybrid analysisJ C Marini, D K Grange, G S Gottesman, et al.Pageof 4