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Humangenetik|September 23, 1975
Familial translocation t(3p-;21q+) associated with both Down's and Sturge-Weber's syndrome in unbalanced stateM Habedank, G KampeHumangenetik|January 1, 1975
Lipoproteins in lecithin-cholesterol-acyltransferase(LCAT)-deficiency. II. Further studies on the abnormal high-density-lipoproteinsG Utermann, H J Menzel, K H Langer, et al.Humangenetik|January 1, 1975
Enzyme polymorphisms and haemoglobin variants in GreeksP Schneider, R Aanthakrishnan, H Walter, et al.Humangenetik|October 20, 1975
Prenatal diagnosis of I-cell diseaseI Matsuda, S Arashima, T Mitsuyama, et al.Humangenetik|January 1, 1975
Frequency and distribution of sister-chromatid exchanges in a case of Fanconi's anemiaK Sperling, R D Wegner, H Riehm, et al.Humangenetik|October 7, 1975
Glucose phosphate isomerase deficiency with hereditary hemolytic anemia in a Spanish family: clinical and familial studiesJ L Vives-Corrons, C Rozman, A Kahn, et al.Humangenetik|January 1, 1975
On the geographical distribution of pseudocholinesterase variantsH SteegmüllerHumangenetik|August 29, 1975
Variation in trypsin banding at different stages of contraction in human chromosomes and the definition, by measurement, of the "average" karyotypeM Seabright, P Cooke, M WheelerPageof 23