Chambon, Pascal
Centre Hospitalier Universitaire de Rouen
2 papers on CoChatORCID 0000-0002-9040-3051
Most cited papers
- Verified
YY1 haploinsufficiency causes an intellectual disability syndrome featuring transcriptional and chromatin dysfunction
Gabriele, M., Vulto-van Silfhout, A. T., Germain, P.-L., Vitriolo, A., Kumar, R., Douglas, E., Haan, E., Kosaki, K., Takenouchi, T., Rauch, A., et al. (2017) · The American Journal of Human Genetics
Genetics and Neurodevelopmental DisordersGenomics and Rare Diseases
Cited by 163
- Verified
Pregnancy outcomes of prenatally diagnosed Turner syndrome: a French multicenter retrospective study including a series of 975 cases
Gruchy, N., Vialard, F., Blondeel, E., Le Meur, N., Joly‐Hélas, G., Chambon, P., Till, M., Herbaut‐Graux, M., Vigouroux‐Castera, A., Coussement, A., et al. (2014) · Prenatal Diagnosis
Prenatal Screening and DiagnosticsGenetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
Cited by 29
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