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Journal De Genetique Humaine|September 1, 1989
[Truncus arteriosus: an autosomal recessive disease?]B le Marec, S Odent, C Almange, et al.Prenatal Diagnosis|July 1, 1986
Prenatal diagnosis of familial tuberous sclerosis following detection of cardiac rhabdomyoma by ultrasoundH Journel, M Roussey, M H Plais, et al.Journal De Genetique Humaine|January 1, 1989
[Argininosuccinic aciduria. A new case revealed by psychiatric disorders]S Odent, M Roussey, H Journel, et al.American Journal of Medical Genetics|December 1, 1989
MCA/MR syndrome with oligodactyly and Möbius anomaly in first cousins: new syndrome or familial facial-limb disruption sequence?H Journel, M Roussey, B Le MarecJournal De Genetique Humaine|December 1, 1987
[What genetic risk should suggest prenatal diagnosis for cystic fibrosis?]H Journel, M Roussey, B Le MarecJournal De Gynecologie, Obstetrique Et Biologie De La Reproduction|January 1, 1985
[Abnormalities of the neural tube in twins]H Journel, M Roussey, A Dabadie, et al.Journal De Genetique Humaine|August 1, 1986
[Incidence of occult lumbro-sacral spina bifida in parents of children with spina bifida (concerning 80 pairs of parents with affected children)]A Carsin, H Journel, M Roussey, et al.Revue D'Epidemiologie Et De Sante Publique|January 1, 1986
[Evaluation of the incidence of anencephaly and spina bifida in Brittany (1975-1984)]H Journel, B Le Marec, P Parent, et al.Journal De Genetique Humaine|December 1, 1989
["Genetic emergencies" in a pediatric intensive care service]S Odent, P Betremieux, G Defawe, et al.Annales De Genetique|January 1, 1985
Trisomy 11p15 and Beckwith-Wiedemann syndrome. Report of two new casesH Journel, J Lucas, C Allaire, et al.Pageof 32