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Journal De Genetique Humaine|December 1, 1980
Duchenne muscular dystrophy: systematic neonatal screening and earlier detection of carriersH Plauchu, C Dellamonica, J Cotte, et al.Journal De Genetique Humaine|December 1, 1980
[Phenotype of a ring-chromosome 6 carrier. Clinical and cytogenetic study]F Cruz-Marin, S Gilgenkrantz, M J Gregoire, et al.Journal De Genetique Humaine|March 1, 1981
[Neonatal screening for duchenne myopathy by serum elevation of creatine phosphokinase activity. 5 years experience]H Plauchu, C Dellamonica, B Pascal, et al.Journal De Genetique Humaine|March 1, 1981
[Early clinical and histopathological manifestations in 14 boys showing elevated serum creatine-phosphokinase levels in their first year]P Guibaud, H N Carrier, H Plauchu, et al.Journal De Genetique Humaine|December 1, 1981
[From the genetics of disease to the genetics of behavior]D WidlöcherJournal De Genetique Humaine|March 1, 1980
Diaphragmatic defects, craniofacial dysmorphism, cleft palate and distal limb deformities. - a new lethal syndromeP Goddeeris, J P Fryns, H van den BergheJournal De Genetique Humaine|September 1, 1978
[Chromosome 5q-- in the medullar cells of a patient with anaemia which later developed into acute non-differentiated leukaemia (author's transl)]C Cabrol, R AbeleJournal De Genetique Humaine|September 1, 1978
[Screening for heterozygotes in a large family suffering from Steinert's disease with varying clinical manifestations (author's transl)]J P MarcozJournal De Genetique Humaine|September 1, 1978
[Non-fluorescent Y chromosome in a 45,X/46,XY mosaic (author's transl)]B Kaluzewski, L Jakubowski, T Moruzgala, et al.Journal De Genetique Humaine|September 1, 1978
Supernumerary small chromosomal anomaly: report of three cases including one with a familial inversion of chromosome 5M l Lee, J Schneider, P Wasant, et al.Pageof 47