Items where authors include "Bebin, M."
Up a levelArticle
Blanchet, P., Bebin, M., Bruet, S, et al. (16 more authors) (2017) MYT1L mutations cause intellectual disability and variable obesity by dysregulating gene expression and development of the neuroendocrine hypothalamus. PLoS Genetics, 13 (8). e1006957. ISSN 1553-7390
Proceedings Paper
Zarate, Y.A., Gambello, M., Pandya, A. et al. (19 more authors) (2018) Phenotype and natural history in 49 individuals with SATB2- associated syndrome. In: American Journal of Medical Genetics Part A. 38th Annual David W. Smith Workshop on Malformations and Morphogenesis, 26-29 Aug 2017, Stowe, VT. Wiley , pp. 1526-1527.