Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Yung-Yung Cheng"'
An overview of a 30-year experience with amniocentesis in a single tertiary medical center in Taiwan
Autor:
Yi-Wen Chang, Chia-Ming Chang, Pi-Lin Sung, Ming-Jie Yang, Wai Hou Li, Hsin-Yang Li, Ling-Chao Chen, Ling-Yi Cheng, Yu-Ling Lai, Yung-Yung Cheng, Wen-Hsun Chang, Kuan-Chong Chao, Peng-Hui Wang
Publikováno v:
Taiwanese Journal of Obstetrics & Gynecology, Vol 51, Iss 2, Pp 206-211 (2012)
Objective: Amniocentesis is a popular and effective prenatal diagnostic tool for chromosomal disorders. It is well-established that the risk of chromosomal abnormalities increases with maternal age; however, other related indications are seldom repor
Externí odkaz:
https://doaj.org/article/a63173d3e25245d8bf9c7e7cb20a6302
Autor:
Pi-Lin Sung, Chia-Ming Chang, Chih-Yao Chen, Peng-Hui Wang, Kuan-Chong Chao, Kuo-Chang Wen, Yung-Yung Cheng, Yueh-Chun Li, Chyi-Chyang Lin
Publikováno v:
Taiwanese Journal of Obstetrics & Gynecology, Vol 51, Iss 2, Pp 260-265 (2012)
Objective: To present a prenatal diagnosis of microdeletion 16p13.11 with partial monosomy of 2q37.1-qter and partial trisomy of 7p15.3-pter in a fetus with bilateral ventriculomegaly, agenesis of corpus callosum, and polydactyly. Case Report: A 41-y
Externí odkaz:
https://doaj.org/article/043d4969ccd94cdc88453718c78f5fc6
Autor:
Wen-Hsun Chang, Ming-Jie Yang, Shiau-You Wang, Ling-Chao Chen, Ming-Shyen Yen, Yi-Wen Chang, Kuan-Chong Chao, Ling-Yi Cheng, Chia-Ming Chang, Chang-Ching Yeh, Yu-Ling Lai, Yung-Yung Cheng, Pi-Lin Sung, Shang-Rong Chen, Wai Hou Li, Peng-Hui Wang
Publikováno v:
Journal of the Chinese Medical Association, Vol 76, Iss 3, Pp 153-157 (2013)
Background Reciprocal translocation is the most common type of translocation; however, there are only a few studies that address the indications for reciprocal translocation in amniocentesis. Here we share our data, based on 30 years' experience in a
Autor:
Yueh-Chun Li, Chih-Yao Chen, Pi-Lin Sung, Chia-Ming Chang, Yung-Yung Cheng, Kuo Chang Wen, Kuan-Chong Chao, Chyi-Chyang Lin, Peng-Hui Wang
Publikováno v:
Taiwanese Journal of Obstetrics & Gynecology, Vol 51, Iss 2, Pp 260-265 (2012)
Objective To present a prenatal diagnosis of microdeletion 16p13.11 with partial monosomy of 2q37.1-qter and partial trisomy of 7p15.3-pter in a fetus with bilateral ventriculomegaly, agenesis of corpus callosum, and polydactyly. Case Report A 41-yea