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American Journal of Medical Genetics|April 1, 1983
Brief clinical report: HARD (+/- E) syndrome: report of a sixth family with support for autosomal-recessive inheritanceS Aymé, J F MatteiJournal of Medical Genetics|December 1, 1983
Syndrome of polydactyly, cleft lip, lingual hamartomas, renal hypoplasia, hearing loss, and psychomotor retardation: variant of the Mohr syndrome or a new syndrome?J F Mattei, S AyméAmerican Journal of Human Genetics|March 1, 1984
HLA and trisomy 21. Confirmation of a trend of restricted HLA heterogeneity in parents of Down syndrome childrenS Aymé, P Mercier, R Dallest, et al.American Journal of Medical Genetics|January 1, 1982
GENTIC: a computerized medical genetic case record systemS Aymé, Y Aurran, J Gouvernet, et al.Journal De Genetique Humaine|June 1, 1981
[Individual variability of associations between acrocentrics (author's transl)]M G Mattei, N Souiah, S Aymé, et al.Human Genetics|February 29, 1976
Nonrandom distribution of chromosome breaks in cultured lymphocytes of normal subjectsS Aymé, J F Mattei, M G Mattei, et al.Journal of Medical Genetics|October 1, 1979
Duchenne type muscular dystrophy and consanguinity: difficulties in pedigree analysisS Aymé, J F Pelissier, J M Garnier, et al.Prenatal Diagnosis|April 1, 1992
Prenatal diagnosis of Fryns' syndromeM C Pellissier, N Philip, A Potier, et al.Annales De Biologie Clinique|January 1, 1988
[Neonatal screening for phenylketonuria and hypothyroidism in France. A 12-year experience]M L BriardArchives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|May 10, 2002
[Genetic screening in children]M L BriardPageof 28