Molecular genetic characterization of a prenatally detected de novo interstitial deletion of chromosome 2q (2q31.1-q32.1) encompassing HOXD13, ZNF385B and ZNF804A associated with syndactyly and increased first-trimester nuchal translucency
Keywords: Chromosome 2q31.1q32.1 deletion; HOXD13; Nuchal translucency; Prenatal diagnosis; Syndactyly;