| Prenatal diagnosis of microdeletion 16p13.11 combination with partialmonosomy of 2q37.1-qter and partial trisomy of 7p15.3-pter in a fetus withbilateral ventriculomegaly, agenesis of corpus callosum, and polydactyly |
Sung, P.L.;Chang, C.M.;Chen, C.Y.;Wang, P.H.;Chao, K.C.;Wen, K.C.;Cheng, Y.Y.;Li, Y.C.;Lin, C.C.; |
Taiwanese Journal of Obstetrics and Gynecology |
2012-06-01 |
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