Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Chung-Hu Fu"'
Autor:
Chih-Ping Chen, Chung-Hu Fu, Yi-Hui Lin, Schu-Rern Chern, Peih-Shan Wu, Yen-Ni Chen, Shin-Wen Chen, Wayseen Wang
Publikováno v:
Taiwanese Journal of Obstetrics & Gynecology, Vol 55, Iss 6, Pp 871-873 (2016)
Objective: We present prenatal diagnosis of familial transmission of 17q12 duplication associated with no apparent phenotypic abnormality. Case Report: A 36-year-old woman underwent amniocentesis at 17 weeks of gestation because of advanced maternal
Externí odkaz:
https://doaj.org/article/0091f15f4bed47b485a2a51dbeaa2ec3
Autor:
Chih-Ping Chen, Chung-Hu Fu, Schu-Rern Chern, Peih-Shan Wu, Jun-Wei Su, Chen-Chi Lee, Meng-Shan Lee, Wayseen Wang
Publikováno v:
Taiwanese Journal of Obstetrics & Gynecology, Vol 52, Iss 3, Pp 401-406 (2013)
Objective: To present prenatal diagnosis of partial monosomy 5p (5p14.1 → pter) and partial monosomy 14q (14q32.31 → qter). Materials and Methods: A 33-year-old woman underwent amniocentesis at 20 weeks of gestation because of abnormal fetal ultr
Externí odkaz:
https://doaj.org/article/bdd9198895e44a7093e5b6b320399655
Autor:
Chung-Hu Fu, Jun-Wei Su, Peih-Shan Wu, Meng-Shan Lee, Chih-Ping Chen, Wayseen Wang, Schu-Rern Chern, Chen-Chi Lee
Publikováno v:
Taiwanese Journal of Obstetrics & Gynecology, Vol 52, Iss 3, Pp 401-406 (2013)
Objective To present prenatal diagnosis of partial monosomy 5p (5p14.1 → pter) and partial monosomy 14q (14q32.31 → qter). Materials and Methods A 33-year-old woman underwent amniocentesis at 20 weeks of gestation because of abnormal fetal ultras
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d40b455f02a3b1002550539faab5e52
https://doi.org/10.1016/j.tjog.2013.06.005
https://doi.org/10.1016/j.tjog.2013.06.005
Autor:
Yi Hui Lin, Peih Shan Wu, Yen Ni Chen, Shin Wen Chen, Chung Hu Fu, Wayseen Wang, Chih-Ping Chen, Schu Rern Chern
Publikováno v:
Taiwanese Journal of Obstetrics & Gynecology, Vol 55, Iss 6, Pp 871-873 (2016)
Objective We present prenatal diagnosis of familial transmission of 17q12 duplication associated with no apparent phenotypic abnormality. Case Report A 36-year-old woman underwent amniocentesis at 17 weeks of gestation because of advanced maternal ag
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::84ae9c2248e08e317359cb7e5a803566
https://pubmed.ncbi.nlm.nih.gov/28040137
https://pubmed.ncbi.nlm.nih.gov/28040137