Laurence Michel‐Calemard

Genotype-phenotype analysis in 2,405 patients with a dystrophinopathy using the UMD-DMD database: a model of nationwide knowledgebase

Sylvie Tuffery‐Giraud, Christophe Béroud, France Leturcq et al. · Human Mutation · 2009 · 364 citations · Full text

Genetics, Databases, Diagnosis +26

Evaluation of Gonadal Function in 107 Intersex Patients by Means of Serum Antimüllerian Hormone Measurement¹

Rodolfo A. Rey, Corinne Belville, Claire Nihoul‐Feketé et al. · The Journal of Clinical Endocrinology & Metabolism · 1999 · 202 citations · Full text

Aerosol Administration of a Recombinant Adenovirus Expressing CFTR to Cystic Fibrosis Patients: A Phase I Clinical Trial

G. Bellon, Laurence Michel‐Calemard, Danièle Thouvenot et al. · Human Gene Therapy · 1997 · 176 citations

Gonadal Dysgenesis Without Adrenal Insufficiency in a 46, XY Patient Heterozygous for the Nonsense C16X Mutation: A Case of SF1 Haploinsufficiency

Delphine Mallet, Patricia Bretones, Laurence Michel‐Calemard et al. · The Journal of Clinical Endocrinology & Metabolism · 2004 · 140 citations · Full text

Genotype–phenotype correlations in fetuses and neonates with autosomal recessive polycystic kidney disease

Érick Denamur, Anne‐Lise Delezoide, Corinne Alberti et al. · Kidney International · 2009 · 91 citations

Genetic Disorder, Medicine, Genetics +9