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Journal De Genetique Humaine|March 1, 1976
[Translocation 46,XY,t(2;5) (q37;q14) and mental retardation. Clinical and cytogenetic study]S Gilgenkrantz, R Walbaum, G Mauuary, et al.Journal De Genetique Humaine|December 1, 1977
[Two monozygotic twin sisters affected with a severe form of osteogenesis imperfecta congenita (author's transl)]J N Le Frèche, C Le Gouguec, B Le MarecJournal De Genetique Humaine|December 1, 1979
[V.A.T.E.R. association and its limits]J L Fournier, J Jacquemin, J Farriaux, et al.Journal De Genetique Humaine|December 1, 1979
[Septo-optic dysplasia: clinical study and elements of genetic counseling]P Landrieu, P EvrardJournal De Genetique Humaine|December 1, 1983
Unusual morphodysplasia as a result of early amnion rupture: umbilico-cephalic adherenceD Chappard, B LaurasJournal De Genetique Humaine|March 1, 1978
[Haemoglobinosis C/beta-thalassemia double heterozygosity in an Algerian patient with total suppression of haemoglobin A synthesis (author's transl)]G Boreux, J J Farquet, P Pugin, et al.Journal De Genetique Humaine|March 1, 1978
Ovarian differentiation in Turner's syndromeC F Rivelis, R Coco, C BergadaJournal De Genetique Humaine|March 1, 1978
Prevalence of Klinefelter's syndrome (47,XXY) in a general male populationE Zeuthen, J NielsenJournal De Genetique Humaine|June 1, 1978
[Do all cases of trisomy 18 with long survival (beyond 10 years) show mosaicism in fibroblasts? (author's transl)]L Crippa, J P Marcoz, D Klein, et al.Journal De Genetique Humaine|December 1, 1976
Evolution of human cytogenetics: an encyclopedic essay. III. The second decade after 1956: banding techiquesP K Srivastava, F V LucasPageof 47