"Sensitivity"@en . "Inherited metabolic diseases"@en . . . "Precision medicine"@en . "Oculoauriculofrontonasal syndrome"@en . . "INHBA"@en . "Alpha-latrotoxin"@en . "Rhombencephalosynapsis"@en . <0000-0002-8333-1360> . "Next-generation sequencing"@en . <150719892> . . . . "Panel"@en . "Activin"@en . "Adhesion-GPCR"@en . "Genomics"@en . "Polyhydramnios"@en . "6239a939d30e8e87eddc0321f6fc6001" . "Hiv-1" . "ADGRL2"@en . "Exome"@en . "\u00C9pissage alternatif" . "Non-immune hydrops fetalis"@en . "Whole genome sequencing"@en . "Cancer"@en . . "INHA"@en . "Frontonasal dysplasia"@en . "Alternative splicing"@en . "Ovary"@en . "Vih-1" . . "Bioinformatics"@en . "Hydrops fetalis"@en . "Constraints"@en . "Vezain" . . "Read-depth information"@en . . "Prenatal diagnosis"@en . "LPHN2"@en . . "Qualitative reasoning"@en . . "Human extreme microcephaly"@en . "CNVs detection"@en . "Modelling" . "Myriam" . . . . "Myriam Vezain" . "Inhibin"@en . "Mod\u00E9lisation" . "Hybrid system"@en . . . "CANOES"@en . "Inborn errors of metabolism"@en . "Whole exome sequencing"@en .