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Journal De Genetique Humaine|September 1, 1985
[Evaluation of 100 autopsies performed in the maternity service of the Hôtel-Dieu in Lyon during an 18 month period]M P Cordier, G Sournies, Y Domenichini, et al.
Journal De Genetique Humaine|December 1, 1978
Familial Y/22 translocation in a womanP R de Chieri
Journal De Genetique Humaine|November 1, 1978
[Morphologic and dermatoglyphic aspects of Klinefelter 47,XXY syndrome (author's transl)]R Pétremand-Hyvärinen
Journal De Genetique Humaine|June 1, 1979
[Hereditary demyelinating diseases - the leukodystrophies]J François
Journal De Genetique Humaine|August 1, 1986
[Prenatal diagnosis of genetic diseases using chorionic villi]J Boué, C Deluchat, H Nicolas, et al.
Journal De Genetique Humaine|August 1, 1986
[Genetic study of spinocerebellar hereditary degenerations in Tunisia. Role of consanguinity in their occurrence]M Ben Hamida, H Chaabouni, S Madani, et al.
Journal De Genetique Humaine|August 1, 1986
[Genetic study of eight cases of spondylo-epiphyseal dysplasia tarda and its autosomal recessive transmission]H Chaabouni, H Douiri, M M Abdelkefi, et al.
Journal De Genetique Humaine|August 1, 1986
[Reinfection after rubella and congenital polymalformation syndrome]G Sibille, P Sarda, J Jalaguier, et al.
Journal De Genetique Humaine|August 1, 1986
Trisomy 6qter resulting from a familial (6;10) (q23;q26) translocationM A Enriquez-Guerra, H Rivera, M Moller, et al.
Journal De Genetique Humaine|August 1, 1986
Pericentric inversions of the X chromosome. A new observation and review of the published casesR A Pfeiffer, M Kossakiewicz, C Baisch
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