Homozygous silencing of T-box transcription factor EOMES leads to microcephaly with polymicrogyria and corpus callosum agenesisBAALA, Lekbir; BRIAULT, Sylvain; ATTIE-BITACH, Tania et al.Nature genetics. 2007, Vol 39, Num 4, pp 454-456, issn 1061-4036, 3 p.Article

OTX2 mutations contribute to the otocephaly-dysgnathia complexCHASSAING, Nicolas; SORRENTINO, Susanna; VIGOUROUX, Adeline et al.Journal of medical genetics. 2012, Vol 49, Num 6, pp 373-379, issn 0022-2593, 7 p.Article

Loss-of-Function Mutation in the Dioxygenase-Encoding FTO Gene Causes Severe Growth Retardation and Multiple MalformationsBOISSEL, Sarah; REISH, Orit; ETCHEVERS, Heather C et al.American journal of human genetics. 2009, Vol 85, Num 1, pp 106-111, issn 0002-9297, 6 p.Article

Matthew-Wood syndrome is caused by truncating mutations in the retinol-binding protein receptor gene STRA6GOLZIO, Christelle; MARTINOVIC-BOURIEL, Jelena; VEKEMANS, Michel et al.American journal of human genetics. 2007, Vol 80, Num 6, pp 1179-1187, issn 0002-9297, 9 p.Article

Highly conserved non-coding elements on either side of SOX9 associated with Pierre Robin sequenceBENKO, Sabina; FANTES, Judy A; MCBRIDE, David et al.Nature genetics. 2009, Vol 41, Num 3, pp 359-364, issn 1061-4036, 6 p.Article

Human neural crest cells display molecular and phenotypic hallmarks of stem cellsTHOMAS, Sophie; THOMAS, Marie; WINCKER, Patrick et al.Human molecular genetics (Print). 2008, Vol 17, Num 21, pp 3411-3425, issn 0964-6906, 15 p.Article

Cytogenetic and histological features of a human embryo with homogeneous chromosome 8 trisomyGOLZIO, Christelle; GUIRCHOUN, Jessica; OZILOU, Catherine et al.Prenatal diagnosis. 2006, Vol 26, Num 13, pp 1201-1205, issn 0197-3851, 5 p.Article

Human neural tube defects : Developmental biology, epidemiology, and geneticsDETRAIT, Eric R; GEORGE, Timothy M; ETCHEVERS, Heather C et al.Neurotoxicology and teratology. 2005, Vol 27, Num 3, pp 515-524, issn 0892-0362, 10 p.Article

SNPs in the neural cell adhesion molecule 1 gene (NCAM1) may be associated with human neural tube defectsDEAK, Kristen L; BOYLES, Abee L; MCCLAY, David et al.Human genetics. 2005, Vol 117, Num 2-3, pp 133-142, issn 0340-6717, 10 p.Article