S. Aymé

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Syndrome of polydactyly, cleft lip, lingual hamartomas, renal hypoplasia, hearing loss, and psychomotor retardation: variant of the Mohr syndrome or a new syndrome?

J. Mattéi, S. Aymé, 1983, Journal of medical genetics.

HLA and trisomy 21. Confirmation of a trend of restricted HLA heterogeneity in parents of Down syndrome children.

J. Mattéi, P. Mercier, S. Aymé, 1984, American journal of human genetics.

Nonrandom distribution of chromosome breaks in cultured lymphocytes of normal subjects

M. Mattei, J. Mattéi, Y. Aurran, 1976, Human Genetics.

Phenotype-genotype correlations in X linked retinitis pigmentosa.

P. Lefrançois, D. Bonneau, C. Martin, 1992, Journal of medical genetics.

Prenatal diagnosis of Fryns' syndrome

N. Philip, S. Aymé, J. Mattéi, 1992, Prenatal diagnosis.

Protocols to establish genotype-phenotype correlations in Down syndrome.

E. Courchesne, C. Epstein, J. Korenberg, 1991, American journal of human genetics.

Quantitative and qualitative study of acrocentric associations in 109 normal subjects

M. Mattei, J. Gouvernet, J. Mattéi, 1976, Human Genetics.

A dynamic study in two new cases of X chromosome translocations

M. Mattei, J. Mattéi, F. Giraud, 1978, Human Genetics.

Abnormal childhood phenotypes associated with the same balanced chromosome rearrangements as in the parents

M. Mattei, J. Mattéi, F. Giraud, 1979, Human Genetics.

Genetic Services in France

M. Briard, J. Mattei, S. Aymé, 1997, European journal of human genetics : EJHG.

Duchenne type muscular dystrophy and consanguinity: difficulties in pedigree analysis.

J. Garnier, J. Mattéi, J. Pelissier, 1979, Journal of medical genetics.

Epilepsy, antiepileptic drugs, and malformations in children of women with epilepsy: a French prospective cohort study.

G. Trentin, P. Genton, R. Guerrini, 1992, Neurology.