Kitzis, Alain

Université de Poitiers · Centre Hospitalier Universitaire de Poitiers

1 paper on CoChatORCID 0000-0001-7533-1398

Most cited papers

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Molecular and clinical characterization of 25 individuals with exonic deletions of NRXN1 and comprehensive review of the literature
Béna, F., Bruno, D. L., Eriksson, M., van Ravenswaaij‐Arts, C., Stark, Z., Dijkhuizen, T., Gerkes, E., Gimelli, S., Ganesamoorthy, D., Thuresson, A. C., et al. (2013) · American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
Genetics and Neurodevelopmental DisordersGenomic variations and chromosomal abnormalities
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