Anne-Lorraine Tellier

PAX2 mutations in oligomeganephronia

Rémi Salomon, Anne-Lorraine Tellier, Tania Attié‐Bitach et al. · Kidney International · 2001 · 120 citations · Full text

Pax2 Mutations, Genetic Disorder, Genetics +4

PAX2 mutations in renal–coloboma syndrome: mutational hotspot and germline mosaicism

Jeanne Amiel, Sophie Audollent, Dominique Joly et al. · European Journal of Human Genetics · 2000 · 79 citations · Full text

Pax2 Mutations, Urology, Genetic Disorder +5

Expression of thePAX2 gene in human embryos and exclusion in the CHARGE syndrome

Anne-Lorraine Tellier, Jeanne Amiel, Anne‐Lise Delezoide et al. · American Journal of Medical Genetics · 2000 · 60 citations · Full text

Genetics, Pathology, Molecular Genetics +17

Features of DiGeorge syndrome and CHARGE association in five patients.

Pascale de Lonlay-Debeney, Valérie Cormier‐Daire, Jeanne Amiel et al. · Journal of Medical Genetics · 1997 · 59 citations · Full text

Developmental Anomaly, Rare Diseases, Digeorge Syndrome +11

Increased paternal age in CHARGE association

Anne-Lorraine Tellier, Stanislas Lyonnet, Valérie Cormier‐Daire et al. · Clinical Genetics · 1996 · 45 citations