"Polyhydramnios"@en . "Precision medicine"@en . "Clinical laboratory techniques"@en . "a891e3cff016b3915c03993fdc932b66" . "Coutant" . "Adhesion-GPCR"@en . "Genetic predisposition to disease"@en . "Alpha-latrotoxin"@en . . "Next-generation sequencing"@en . "High-throughput DNA sequencing"@en . . "Activin"@en . "Sophie Coutant" . "Non-immune hydrops fetalis"@en . "ADGRL2"@en . . "Heart and brain malformation"@en . "Neoplasia"@en . "Panel"@en . "Sophie" . . . "Read-depth information"@en . . "Rhombencephalosynapsis"@en . "Skin"@en . . . "CNVs detection"@en . . . . "Myositis and muscle disease"@en . "Inhibin"@en . "Muscle"@en . . . "Cancer"@en . . "LPHN2"@en . "Plant exDNA"@en . . . "Genetics"@en . "Nonsense mediated decay"@en . "Bioinformatics"@en . "CANOES"@en . "Genomics"@en . "Inherited metabolic diseases"@en . "Root extracellular trap RET"@en . . . "Exome"@en . "Methods"@en . "INHBA"@en . "Hydrops fetalis"@en . . "PEP-13"@en . "Inborn errors of metabolism"@en . "INHA"@en . "Sensitivity"@en . . "SMG9"@en . "Exome sequencing"@en . . . "CDX2 de novo mutation"@en . "Germ-line mutation"@en . "Audal dysgenesis"@en . "Ovary"@en . . "Prenatal diagnosis"@en . "Sirenomelia"@en . "Human extreme microcephaly"@en . "Glycine max L Merr"@en . "Genetic testing"@en .