https://data.archives-ouvertes.fr/author/763847

https://data.archives-ouvertes.fr/author/763847

http://xmlns.com/foaf/0.1/interest https://data.archives-ouvertes.fr/subject/sdv.neu.nb
http://xmlns.com/foaf/0.1/topic_interest OCNDS
http://xmlns.com/foaf/0.1/topic_interest Penetrance
http://xmlns.com/foaf/0.1/topic_interest Missense variant
http://www.w3.org/2002/07/owl#sameAs 0000-0002-5953-2728
http://xmlns.com/foaf/0.1/topic_interest Infantile
http://xmlns.com/foaf/0.1/topic_interest MECP2duplication syndrome
http://xmlns.com/foaf/0.1/topic_interest X-linked
http://xmlns.com/foaf/0.1/topic_interest MicroRNAs
http://xmlns.com/foaf/0.1/topic_interest Episignature
http://xmlns.com/foaf/0.1/topic_interest Genotype-phenotype correlation
http://xmlns.com/foaf/0.1/topic_interest Magnetic Resonance Imaging
http://xmlns.com/foaf/0.1/topic_interest PTHS
http://xmlns.com/foaf/0.1/topic_interest NDD-neurodevelopmental disorder
http://xmlns.com/foaf/0.1/topic_interest SNPs
http://xmlns.com/foaf/0.1/topic_interest ADGRG2
http://xmlns.com/foaf/0.1/interest https://data.archives-ouvertes.fr/subject/sdv.gen.gh
http://xmlns.com/foaf/0.1/interest https://data.archives-ouvertes.fr/subject/scco.neur
http://xmlns.com/foaf/0.1/topic_interest High throughput data mining
http://xmlns.com/foaf/0.1/topic_interest Incidental findings
http://xmlns.com/foaf/0.1/topic_interest EpiSign
http://xmlns.com/foaf/0.1/topic_interest SPINK1
http://xmlns.com/foaf/0.1/topic_interest Mono-allelic expression
http://xmlns.com/foaf/0.1/topic_interest POBINDS
http://xmlns.com/foaf/0.1/topic_interest Congenital absence of vas deferens
http://xmlns.com/foaf/0.1/topic_interest RhoA GTPase
http://xmlns.com/foaf/0.1/name Thierry Bienvenu
http://xmlns.com/foaf/0.1/topic_interest Male infertility
http://xmlns.com/foaf/0.1/topic_interest Migration
http://xmlns.com/foaf/0.1/topic_interest Xq28 duplication
http://xmlns.com/foaf/0.1/interest https://data.archives-ouvertes.fr/subject/sdv.mhep.psm
http://xmlns.com/foaf/0.1/topic_interest Genotype/phenotype correlations
http://xmlns.com/foaf/0.1/interest https://data.archives-ouvertes.fr/subject/sdv.sp
http://xmlns.com/foaf/0.1/topic_interest Neurodevelopmental disorder
http://xmlns.com/foaf/0.1/topic_interest Oligophrenin-1
http://xmlns.com/foaf/0.1/interest https://data.archives-ouvertes.fr/subject/sdv.bibs
http://xmlns.com/foaf/0.1/topic_interest TCF4
http://xmlns.com/foaf/0.1/topic_interest Obstructive azoospermia
http://xmlns.com/foaf/0.1/topic_interest CFTR
http://xmlns.com/foaf/0.1/topic_interest Molecular diagnostics
http://xmlns.com/foaf/0.1/topic_interest Facial dysmorphism
http://xmlns.com/foaf/0.1/familyName Bienvenu
http://xmlns.com/foaf/0.1/topic_interest Morphology
http://xmlns.com/foaf/0.1/topic_interest CTRC
http://xmlns.com/foaf/0.1/topic_interest VUS classification
http://xmlns.com/foaf/0.1/topic_interest Pitt-Hopkins syndrome
http://xmlns.com/foaf/0.1/topic_interest Genetic counseling
http://xmlns.com/foaf/0.1/topic_interest Astrocyte
http://xmlns.com/foaf/0.1/topic_interest Nonvisualization of the fetal gallbladder
http://xmlns.com/foaf/0.1/topic_interest Mutation
http://xmlns.com/foaf/0.1/topic_interest Clinical databases
http://xmlns.com/foaf/0.1/topic_interest IQSEC2
http://xmlns.com/foaf/0.1/interest https://data.archives-ouvertes.fr/subject/info.info-ai
http://xmlns.com/foaf/0.1/topic_interest Diagnosis
http://xmlns.com/foaf/0.1/interest https://data.archives-ouvertes.fr/subject/sdv.bc
http://xmlns.com/foaf/0.1/topic_interest PRSS1
http://xmlns.com/foaf/0.1/firstName Thierry
http://xmlns.com/foaf/0.1/topic_interest Isoforms
http://xmlns.com/foaf/0.1/topic_interest Intellectual disability
http://xmlns.com/foaf/0.1/topic_interest MECP2 gene
http://xmlns.com/foaf/0.1/topic_interest Epilepsy
http://xmlns.com/foaf/0.1/topic_interest Autism spectrum disorders
http://xmlns.com/foaf/0.1/topic_interest MECP2
http://xmlns.com/foaf/0.1/topic_interest DNA methylation
http://xmlns.com/foaf/0.1/topic_interest CK2 casein kinase II
http://xmlns.com/foaf/0.1/topic_interest Cystic Fibrosis
http://xmlns.com/foaf/0.1/topic_interest Genetic counselling
http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://xmlns.com/foaf/0.1/Person
http://xmlns.com/foaf/0.1/topic_interest Pancreatitis
http://xmlns.com/foaf/0.1/topic_interest Rett syndrome
http://xmlns.com/foaf/0.1/topic_interest Uncertain clinical cases
http://xmlns.com/foaf/0.1/interest https://data.archives-ouvertes.fr/subject/sdv.bbm
http://xmlns.com/foaf/0.1/topic_interest MECP2gene
http://xmlns.com/foaf/0.1/topic_interest Ultrasound scan
http://xmlns.com/foaf/0.1/interest https://data.archives-ouvertes.fr/subject/sdv.neu.sc
http://xmlns.com/foaf/0.1/topic_interest X-linked inheritance
http://xmlns.com/foaf/0.1/topic_interest Variant classification
http://xmlns.com/foaf/0.1/topic_interest Prenatal diagnosis
http://xmlns.com/foaf/0.1/topic_interest Autism-spectrum disorders ASD
https://aurehal.archives-ouvertes.fr/author/763847

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