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Human Genetics|February 1, 1992
Carrier detection and prenatal diagnosis of cystic fibrosis using an intragenic TA-repeat polymorphismE Mornet, C Chateau, B Simon-Bouy, et al.Prenatal Diagnosis|July 1, 1993
First-trimester free beta (hCG) screening for Down syndromeJ N Macri, K Spencer, D Aitken, et al.Prenatal Diagnosis|January 1, 1981
Prenatal diagnosis of congenital enzymopenic methaemoglobinaemia with mental retardation due to generalized cytochrome b5 reductase deficiency: first report of two casesC Junien, A Leroux, D Lostanlen, et al.Lancet (London, England)|February 20, 1988
Genetic differences between cystic fibrosis with and without meconium ileusE Mornet, B Simon-Bouy, J L Serre, et al.Clinical Genetics|February 1, 1989
Genetic heterogeneity between two clinical forms of cystic fibrosis evidenced by familial analysis and linked DNA probesE Mornet, B Simon-Bouy, J L Serre, et al.Prenatal Diagnosis|July 1, 1989
Early prenatal diagnosis of 21-hydroxylase deficiency using amniotic fluid 17-hydroxyprogesterone determination and DNA probesM Raux-Demay, E Mornet, J Boue, et al.Endocrinology|May 1, 1984
17 beta-Hydroxysteroid dehydrogenase activity in human breast epithelial cell and fibroblast culturesJ F Prud'homme, C Malet, A Gompel, et al.Prenatal Diagnosis|October 1, 1994
Amniotic fluid digestive enzymes: diagnostic value in fetal gastrointestinal obstructionsF Muller, M Dommergues, Y Ville, et al.La Nouvelle Presse Medicale|February 21, 1981
[Removal of kidneys for transplantation. Experience in a French general teaching hospital (author's transl)]T Nebout, P Romano, C Abbou, et al.The EMBO Journal|June 1, 1988
Isolation of a human gene with protein sequence similarity to human and murine int-1 and the Drosophila segment polarity mutant winglessB J Wainwright, P J Scambler, P Stanier, et al.Pageof 5