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Molecular and Cellular Probes|June 1, 1992
Comparison of spot-blot and microtitre plate methods for the detection of HIV-1 PCR productsB Conway, L J Bechtel, K A Adler, 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.Human Heredity|January 1, 1982
Glucose-6-phosphate dehydrogenase and hemoglobin variants in Kel Kummer Tuareg and related groups. Indirect evidence for alpha-thalassemia traitC Junien, A Chaventré, Y Fofana, et al.Clinical Genetics|January 1, 1997
Spectrum of CFTR mutations in Argentine cystic fibrosis patientsL Chertkoff, A Visich, T Bienvenu, et al.Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|August 1, 1993
Deficiency of the 50 kDa dystrophin associated glycoprotein (adhalin) in severe autosomal recessive muscular dystrophies in children native from European countriesM Fardeau, K Matsumura, F M Tomé, et al.Human Genetics|January 1, 1980
PK3: a new chromosome enzyme marker for gene dosage studies in chromosome 15 imbalanceC Junien, H Rubinson-Skala, J C Dreyfus, et al.American Journal of Human Genetics|July 1, 1984
The genes coding for A alpha-, B beta-, and gamma-chains of fibrinogen map to 4q2I Henry, G Uzan, D Weil, et al.American Journal of Human Genetics|May 23, 1998
Mapping of a congenital microcoria locus to 13q31-q32C Rouillac, O Roche, D Marchant, et al.Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|January 1, 1994
Genetic heterogeneity of severe childhood autosomal recessive muscular dystrophy with adhalin (50 kDa dystrophin-associated glycoprotein) deficiencyN B Romero, F M Tomé, F Leturcq, et al.Human Molecular Genetics|April 1, 1996
The hereditary pancreatitis gene maps to long arm of chromosome 7L Le Bodic, J D Bignon, O Raguénès, et al.Pageof 19