M. Gonzalés

Anatomy of the Lamina Cribrosa in Human Eyes

Ronald L. Radius, M. Gonzalés · Archives of Ophthalmology · 1981 · 157 citations

Molecular findings and clinical data in a cohort of 150 patients with anophthalmia/microphthalmia

Nicolas Chassaing, Alexandre Causse, Adeline Vigouroux et al. · Clinical Genetics · 2013 · 117 citations · Full text

Syndromic Am, Ocular Disease, Developmental Biology +14

Mutations in CNTNAP1 and ADCY6 are responsible for severe arthrogryposis multiplex congenita with axoglial defects

Annie Laquerrière, Jérôme Maluenda, Adrien Camus et al. · Human Molecular Genetics · 2013 · 109 citations · Full text

Pns Myelination, Developmental Biology, Autoimmune Disease +14

<i>RET</i> and <i>GDNF</i> mutations are rare in fetuses with renal agenesis or other severe kidney development defects

G. Macé, Mélanie Parisot, Vincent Morinière et al. · Journal of Medical Genetics · 2011 · 64 citations · Full text

Molecular heterogeneity in fetal forms of type II lissencephaly

C Bouchet, M. Gonzalés, Sandrine Vuillaumier‐Barrot et al. · Human Mutation · 2007 · 63 citations