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Journal De Genetique Humaine|June 1, 1983
[Unusual course of alpha-fetoprotein levels in a case of spina bifida detected by prenatal diagnosis]D Augier, M F Sarramon, G Dutau, et al.Journal De Genetique Humaine|June 1, 1988
[Genetic counseling in neurofibromatosis. Apropos of a study of 53 families]A Toutain, J Kaplan, M L Briard, et al.Journal De Genetique Humaine|January 1, 1985
[Osteodysplasia or the Melnick-Needles syndrome; (apropos of a new case)]B Deleporte, J P Buissart, P Vankemmel, et al.Journal De Genetique Humaine|January 1, 1985
[Amniotic disease in the mother and severe heart abnormalities in 2 infants]N CankiJournal De Genetique Humaine|January 1, 1985
[Intercalary de novo deletion of chromosome 1: del(1) (q24 to q32)]C Faugeras, D BartheJournal De Genetique Humaine|January 1, 1985
Trisomy 20p: case report and genetic reviewI W Lurie, N V Rumyantseva, D V Zaletajev, et al.Journal De Genetique Humaine|August 1, 1986
[Requests for prenatal diagnosis from parents of children with cystic fibrosis]G Demay, A C Stubnicer, A Boué, et al.Journal De Genetique Humaine|August 1, 1986
[Transmission of an 18 ring chromosome in two generations in subjects of normal phenotype]C Faugeras, D BartheJournal De Genetique Humaine|August 1, 1986
Autosomal dominant piebaldism and mental retardation syndrome associated with a t(1;2) (p22.1;q36)H Rivera, M C Alvarez-Arratia, M Moller, et al.Journal De Genetique Humaine|March 1, 1978
Multiple ophthalmic anomalies and digital hypoplasiaJ Chemke, M Oliver, D Mallek, et al.Pageof 47