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Journal De Genetique Humaine|December 1, 1985
[Familial adrenoleukodystrophy]J M Le Fur, F Le Meur, P Parent, et al.Journal De Genetique Humaine|December 1, 1987
X-linked mental retardation. I. Martin-Bell syndrome (report of 18 families)M Rocchi, N Archidiacono, G FilippiJournal De Genetique Humaine|December 1, 1987
X-linked mental retardation. II. Renpenning syndrome and other types (report of 14 families)N Archidiacono, M Rocchi, A Rinaldi, et al.Journal De Genetique Humaine|December 1, 1978
Partial trisomy 13q inherited from balanced translocation (5;13) (p14;q13)R Coco, G del ReyJournal De Genetique Humaine|December 1, 1978
The peroneal muscular atrophy syndrome: clinical, genetic, electrophysiological and nerve biopsy studies. I. Clinical, genetic and electrophysiological findings and classificationC J Davis, W G Bradley, R MadridJournal De Genetique Humaine|August 1, 1988
[Biochemical markers of neural tube closure defects during the second half of pregnancy]S Guibaud, C Boisson, A Simplot, et al.Journal De Genetique Humaine|June 1, 1983
[Polysyndactyly with complex cardiopathy. Apropos of 3 cases in the same family]J C Bonneau, H Moirot, C Bastard, et al.Journal De Genetique Humaine|December 1, 1977
[Study of fingerprints in 12 cases of hereditary brachydactyly type C and E (author's transl)]D Gnamey, R Walbaum, G FontaineJournal De Genetique Humaine|October 1, 1979
[Omphalocele: hereditary disease with dominant transmission?]B Le Marec, M Roussey, H Bracq, et al.Journal De Genetique Humaine|March 1, 1976
Excretion of guanidino-derivates in urine of hyperargininemic patientsP Wiechert, J Mortelmans, F Lavinha, et al.Pageof 47