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Journal of Medical Genetics|June 1, 1979
Congenital haemolytic anaemia resulting from glucose phosphate isomerase deficiency: genetics, clinical picture, and prenatal diagnosisA G Whitelaw, P A Rogers, D A Hopkinson, et al.Annals of Human Genetics|March 24, 1999
Susceptibility to spina bifida; an association study of five candidate genesK Morrison, C Papapetrou, F A Hol, et al.Investigative Ophthalmology & Visual Science|January 1, 1993
Aging studies on normal lens using the Scheimpflug slit-lamp cameraK Kashima, B L Trus, M Unser, et al.Genes, Chromosomes & Cancer|October 23, 1997
Cytogenetic analysis of three breast carcinoma cell lines using reverse chromosome paintingJ S Morris, N P Carter, M A Ferguson-Smith, et al.Genomics|September 1, 1996
Glomerular-specific imprinting of the mouse gsalpha gene: how does this relate to hormone resistance in albright hereditary osteodystrophy?C M Williamson, J Schofield, E R Dutton, et al.Somatic Cell and Molecular Genetics|March 1, 1987
Regional localization of carbonic anhydrase genes CA1 and CA3 on human chromosome 8M B Davis, L F West, J H Barlow, et al.Proceedings of the National Academy of Sciences of the United States of America|March 1, 1987
Nucleotide and amino acid sequences of human intestinal alkaline phosphatase: close homology to placental alkaline phosphataseP S Henthorn, M Raducha, Y H Edwards, et al.The Journal of Biological Chemistry|February 25, 1992
COQ2 is a candidate for the structural gene encoding para-hydroxybenzoate:polyprenyltransferaseM N Ashby, S Y Kutsunai, S Ackerman, et al.Journal of Lipid Research|September 1, 1981
Factors regulating the activities of the low density lipoprotein receptor and the scavenger receptor on human monocyte-macrophagesA M Fogelman, M E Haberland, J Seager, et al.Developmental Biology|July 27, 1999
Impaired mammary gland development in Cyl-1(-/-) mice during pregnancy and lactation is epithelial cell autonomousV Fantl, P A Edwards, J H Steel, et al.Pageof 32