about
Pleiotropic Mechanisms Indicated for Sex Differences in AutismReverse Pathway Genetic Approach Identifies Epistasis in Autism Spectrum Disorders.Xp21 deletion in female patients with intellectual disability: Two new cases and a review of the literature.Using medical exome sequencing to identify the causes of neurodevelopmental disorders: Experience of 2 clinical units and 216 patients.Mosaic intragenic deletion of FBN2 and severe congenital contractural arachnodactyly.Heterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and EpilepsyNuclear volume differences between balanced and unbalanced spermatozoa in chromosomal translocation carriers
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Q36192641-AFF16B71-08B2-4807-A257-AF060CA008B5Q36246158-CE8C2EBF-6112-400A-8A38-23EB9691254CQ38445051-481C0A9A-14DD-4F59-A495-34255253D6CCQ48124449-F1560E6E-0A70-45E9-85F1-DA379A76F32FQ48315381-B50AFEA4-ACF0-4663-A146-31D594374F45Q64039319-4DE411B2-43FB-4F98-A6D2-60C40C1CB3A1Q86555249-789A8D57-250C-4392-B7E1-69832DD0E34D
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description
investigador
@es
researcher
@en
wetenschapper
@nl
name
Alinoë Lavillaureix
@en
Alinoë Lavillaureix
@nl
type
label
Alinoë Lavillaureix
@en
Alinoë Lavillaureix
@nl
prefLabel
Alinoë Lavillaureix
@en
Alinoë Lavillaureix
@nl
P31
P496
0000-0002-3727-9530