H. Nicolas

Molecular definition of de novo and genetically transmitted WAGR-associated rearrangements of 11p13

Christian Lavedan, F. Barichard, M Azoulay et al. · Cytogenetics and Cell Genetics · 2008 · 33 citations

Life Sciences, Genetics, Molecular Genetics +17

Molecular analysis of uroporphyrinogen decarboxylase deficiency in a family with two cases of hepatoerythropoietic porphyria.

Hubert de Verneuil, Bernard Grandchamp, Paul‐Henri Roméo et al. · Journal of Clinical Investigation · 1986 · 26 citations · Full text

Life Sciences, Genetics, Molecular Biology +14

Prenatal diagnosis of congenital adrenal hyperplasia (21‐OH deficiency type) by HLA typing

P. Couillin, J Boué, H. Nicolas et al. · Prenatal Diagnosis · 1981 · 22 citations

Life Sciences, Endocrinology, Genetics +11

Prenatal Losses of Trisomy 21

J Boué, C Deluchat, H. Nicolas et al. · Human genetics. Supplement · 1981 · 21 citations

Life Sciences, Genetics, Obstetrics +14

Prenatal diagnosis of congenital enzymopenic methaemoglobinaemia with mental retardation due to generalized cytochrome b₅ reductase deficiency: First report of two cases

Claudine Junien, A Leroux, D. Lostanlen et al. · Prenatal Diagnosis · 1981 · 13 citations

Life Sciences, Biochemistry, Genetics +11