O Raoul

Array-based comparative genomic hybridisation identifies high frequency of cryptic chromosomal rearrangements in patients with syndromic autism spectrum disorders

M-L Jacquemont, Damien Sanlaville, Richard Redon et al. · Journal of Medical Genetics · 2006 · 304 citations · Full text

The meiotic stage of nondisjunction in trisomy 21: determination by using DNA polymorphisms

Stylianos E. Antonarakis, Michael B. Petersen, Melvin G. McInnis et al. · PubMed · 1992 · 202 citations · Full text

Trisomie 21 et superoxyde dismutase-1 (IPO-A)

Pierre‐Marie Sinet, J Couturier, B. Dutrillaux et al. · Experimental Cell Research · 1976 · 174 citations

Genetic Disorder, Genetics, Pathogenesis +5

New insights into genotype–phenotype correlation for GLI3 mutations

Florence Démurger, Amale Ichkou, Soumaya Mougou-Zerelli et al. · European Journal of Human Genetics · 2014 · 121 citations · Full text

Genetics, Genotype–phenotype Correlation, Molecular Genetics +3

Cystathionine beta synthase: Gene dosage effect in trisomy 21

B. Chadefaux, M O Rethoré, O Raoul et al. · Biochemical and Biophysical Research Communications · 1985 · 101 citations

Genetic Disorder, Genetics, Cystathionine Beta Synthase +3