. "OCNDS"@en . "Penetrance"@en . "Missense variant"@en . <0000-0002-5953-2728> . "Infantile"@en . "MECP2duplication syndrome"@en . "X-linked"@en . "MicroRNAs"@en . "Episignature"@en . "Genotype-phenotype correlation"@en . "Magnetic Resonance Imaging"@en . "PTHS"@en . "NDD-neurodevelopmental disorder"@en . "SNPs"@en . "ADGRG2"@en . . . "High throughput data mining"@en . "Incidental findings"@en . "EpiSign"@en . "SPINK1"@en . "Mono-allelic expression"@en . "POBINDS"@en . "Congenital absence of vas deferens"@en . "RhoA GTPase"@en . "Thierry Bienvenu" . "Male infertility"@en . "Migration"@en . "Xq28 duplication"@en . . "Genotype/phenotype correlations"@en . . "Neurodevelopmental disorder"@en . "Oligophrenin-1"@en . . "TCF4"@en . "Obstructive azoospermia"@en . "CFTR"@en . "Molecular diagnostics"@en . "Facial dysmorphism"@en . "Bienvenu" . "Morphology"@en . "CTRC"@en . "VUS classification"@en . "Pitt-Hopkins syndrome"@en . "Genetic counseling" . "Astrocyte"@en . "Nonvisualization of the fetal gallbladder"@en . "Mutation" . "Clinical databases"@en . "IQSEC2"@en . . "Diagnosis" . . "PRSS1"@en . "Thierry" . "Isoforms"@en . "Intellectual disability"@en . "MECP2 gene"@en . "Epilepsy"@en . "Autism spectrum disorders"@en . "MECP2"@en . "DNA methylation"@en . "CK2 casein kinase II"@en . "Cystic Fibrosis"@en . "Genetic counselling"@en . . "Pancreatitis"@en . "Rett syndrome"@en . "Uncertain clinical cases"@en . . "MECP2gene"@en . "Ultrasound scan"@en . . "X-linked inheritance"@en . "Variant classification"@en . "Prenatal diagnosis"@en . "Autism-spectrum disorders ASD"@en .