“…But the syndrome has been known to be associated with structural and chromosomal abnormalities, so fetal chromosome analysis is generally recommended. Chromosomal abnormalities such as a partial trisomy of 3p, 9p, 11q, and 16q and a partial monosomy of 1q, 6p, 11q, 12p, and 13q have been reported as being associated with the syndrome (Ballarati et al, 2007;Chen et al, 1996Chen et al, , 2002aChen et al, , 2002bChen et al, , 2005Chen et al, , 2007Poot et al, 2007;Puhl et al, 2010;van Bever et al, 2005). Partial trisomy 3q was also identified in patients with DWS (de Azevedo Moreira et al, 2005;Ounap et al, 2005).…”