Laïla Rifai

Homozygous Inactivating Mutations in the NKX3-2 Gene Result in Spondylo-Megaepiphyseal-Metaphyseal Dysplasia

Jan Hellemans, Marleen Simon, Annelies Dheedene et al. · The American Journal of Human Genetics · 2009 · 35 citations · Full text

Life Sciences, Genetics, Molecular Genetics +12

Ectodermal dysplasia‐like syndrome with mental retardation due to contiguous gene deletion: Further clinical and molecular delineation of del(2q32) syndrome

Laïla Rifai, Marylin Port‐Lis, Anne‐Claude Tabet et al. · American Journal of Medical Genetics Part A · 2009 · 31 citations

Life Sciences, Genetics, Molecular Genetics +16

Genetic Variations Creating MicroRNA Target Sites in the FXN 3′-UTR Affect Frataxin Expression in Friedreich Ataxia

Simonetta Bandiera, François Cartault, Anne‐Sophie Jannot et al. · PLoS ONE · 2013 · 30 citations · Full text

Life Sciences, Genetics, Neurology +12

Autosomal dominant microtia

Siham Chafai Elalaoui, Imane Cherkaoui Jaouad, Laïla Rifai et al. · European Journal of Medical Genetics · 2010 · 13 citations

Novel point mutation in the NKX2-5 gene in a Moroccan family with atrioventricular conduction disturbance and an atrial septal defect in the oval fossa

Laïla Rifai, W Maazouzi, Abdelaziz Sefiani · Cardiology in the Young · 2006 · 12 citations

Medicine, Genetics, Molecular Genetics +17