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Journal De Genetique Humaine|March 1, 1982
[Acetylcholinesterase of amniotic fluid: application to prenatal diagnosis of neural tube closing defects. I. Quantitative tests]S Guibaud, A Simplot, M Bonnet, et al.Journal De Genetique Humaine|October 1, 1982
[Genetic aspects of autosomal fragile sites. Apropos of 40 Cases]M Guichaoua, M G Matteï, J F Matteï, et al.Journal De Genetique Humaine|October 1, 1982
[Echographic detection of chromosomal anomalies apropos of trisomy 13 and 18]J P Aubry, M C Aubry, R Henrion, et al.Journal De Genetique Humaine|June 1, 1981
[Individual variability of associations between acrocentrics (author's transl)]M G Mattei, N Souiah, S Aymé, et al.Journal De Genetique Humaine|December 1, 1981
[Association, in the same subject, of deletion of the short arm of chromosome 4 (4p-) and of complete deficiency of parahydroxyphenyl-pyruvate oxidase activity in the liver (tyrosinosis)]G Malpuech, J F Mattei, J Gaulme, et al.Journal De Genetique Humaine|March 1, 1976
[Polycystic kidney disease of the newborn in two different sibships]C Stoll, D Willard, P Beauvais, et al.Journal De Genetique Humaine|December 1, 1979
Prevention of neural tube malformation by genetic counselling, and prenatal diagnostic surveillanceK M LaurenceJournal De Genetique Humaine|December 1, 1985
[Sex-linked inheritance in fronto-metaphyseal dysplasia]P BalestrazziPageof 47