Marie-Pierre Vié-Luton

Novel HESX1 Mutations Associated with a Life-Threatening Neonatal Phenotype, Pituitary Aplasia, but Normally Located Posterior Pituitary and No Optic Nerve Abnormalities

Marie‐Laure Sobrier, Mohamad Maghnie, Marie-Pierre Vié-Luton et al. · The Journal of Clinical Endocrinology & Metabolism · 2006 · 83 citations · Full text

Alu-element insertion in the homeodomain of<i>HESX1</i>and aplasia of the anterior pituitary

Marie‐Laure Sobrier, Irène Netchine, Claudine Heinrichs et al. · Human Mutation · 2005 · 65 citations

Developmental Anomaly, Transcriptional Regulation, Developmental Biology +14

Unusual Phenotypic Features in a Patient with a Novel Splice Mutation in the GHRHR Gene

Latifa Hilal, Yassir Hajaji, Marie-Pierre Vié-Luton et al. · Molecular Medicine · 2008 · 34 citations · Full text

Symptomatic Heterozygotes and Prenatal Diagnoses in a Nonconsanguineous Family with Syndromic Combined Pituitary Hormone Deficiency Resulting from Two Novel<i>LHX3</i>Mutations

Marie‐Laure Sobrier, Cécile Brachet, Marie-Pierre Vié-Luton et al. · The Journal of Clinical Endocrinology & Metabolism · 2012 · 30 citations · Full text

Molecular screening of a large cohort of Moroccan patients with congenital hypopituitarism

Nabila Fritez, Marie‐Laure Sobrier, Hinde Iraqi et al. · Clinical Endocrinology · 2014 · 21 citations