Prenatal diagnosis of a familial 5p14.3-p14.1 deletion encompassing CDH18, CDH12, PMCHL1, PRDM9 and CDH10 in a fetus with congenital heart disease on prenatal ultrasoundChih‐Ping Chen, Wayseen Wang, Shih-Ting Lai et al.|Taiwanese Journal of Obstetrics and Gynecology|2018Cited by 25
Prenatal diagnosis of a familial 15q11.2 (BP1-BP2) microdeletion encompassing TUBGCP5, CYFIP1, NIPA2 and NIPA1 in a fetus with ventriculomegaly, microcephaly and intrauterine growth restriction on prenatal ultrasoundChih‐Ping Chen, Wayseen Wang, Sui‐Yuan Chang et al.|Taiwanese Journal of Obstetrics and Gynecology|2018Cited by 16
Prenatal diagnosis of a familial 1q21.1-q21.2 microdeletion in a fetus with polydactyly of left foot on prenatal ultrasoundChih‐Ping Chen, Wayseen Wang, Lifeng Chen et al.|Taiwanese Journal of Obstetrics and Gynecology|2018Cited by 9