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, Wenlin Chen 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, Sui‐Yuan Chang et al.|Taiwanese Journal of Obstetrics and Gynecology|2018Cited by 9
Identification of a novel <scp>HLA</scp>‐B allele, <i>B*07:162</i>, in a Taiwanese individualP.‐L. Chen, C.‐C. Chu, Wei‐Shiung Yang et al.|Tissue Antigens|2013Cited by 4