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