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顯示項目1426-1450 / 3217. (共129頁)
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日期	題名	作者
2013-03	Prenatal diagnosis of a missense mutation of c.2279G>A, Gly760Glu in exon 37 of COL1A2 in a fetus with familial osteogenesis imperfecta type IV and favorable outcome	陳持平(Chih-Ping Chen); (Shuan-Pei Lin); (Yi-Ning Su); (Schu-Rern Chern); (Jun-Wei Su); (Wayseen Wang)*
2005	Prenatal diagnosis of an acardiac amorphous twin and the anomalous co-twin in a monoamniotic twin pregnancy	Chen, CP; Shih, JC; Chang, TY; Chern, SR; Lin, CY; Wang, WS; Tzen, CY
2012-12	Prenatal diagnosis of an interstitial deletion of 10q (10q11.21->q21.1): array comparative genomic hybridization characterization and literature review	陳持平(Chih-Ping Chen); (Yi-Ning Su); (Schu-Rern Chern); (Peih-Shan Wu); (Jun-Wei Su); (Dai-Dyi Town); (Wayseen Wang)*
2009-09	Prenatal diagnosis of and molecular analysis of triploidy in a fetus with intrauterine growth restriction, relative macrocephaly and holoprosencephaly	陳持平(Chih-Ping Chen); (Schu-Rern Chern); 蔡輔仁(Fuu-Jen Tsai); (Chin-Yuan Hsu); (Kevin Ko); (Wayseen Wang)*
2009-09	Prenatal diagnosis of and molecular analysis of trisomy 13 mosaicism	陳持平(Chih-Ping Chen); (Schu-Rern Chern); 蔡輔仁(Fuu-Jen Tsai); (Hung-Hung Lin); (Chen-Wen Pan); (Wayseen Wang)*
2013-03	Prenatal diagnosis of and molecular cytogenetic characterization of a de novo interstitial duplication of 11q (11q22.3->q23.3) associated with abnormal maternal serum biochemistry	陳持平(Chih-Ping Chen); (Yi-Ning Su); (Shuan-Pei Lin); (Schu-Rern Chern); (Jun-Wei Su); (Yu-Ting Chen); (Meng-Shan Lee); (Wayseen Wang)*
2007-06	Prenatal diagnosis of atypical facial clefting should alert amniotic band syndrome and prompt a search for associated amniotic bands and other structural anomalies	陳持平(Chih-Ping Chen)*
2011-06	Prenatal diagnosis of cerebral tubers by magnetic resonance imaging following detection of cardiac rhabdomyomas by prenatal ultrasound in a fetus with a nonsense mutation in the TSC2 gene	陳持平(Chih-Ping Chen); (Yi-Ning Su); (Chin-Yuan Hsu); (Ming-Ren Chen); (Yu-Peng Liu); (Pei-Chen Wu); (Wayseen Wang)*
2015-12	Prenatal diagnosis of chromosome 8p23.1 microdeletion by array comparative genomic hybridization using uncultured amniocytes in a pregnancy associated with fetal partial corpus callosum agenesis and schizencephaly	陳持平(Chih-Ping Chen); (Cheng-Ran Peng); (Tung-Yao Chang); (Wan-Yuo Guo); (Yen-Ni Chen); (Peih-Shan Wu); (Dai-Dyi Town); (Wayseen Wang)*
2005	Prenatal diagnosis of concomitant alobar holoprosencephaly and caudal regression syndrome associated with maternal diabetes	Chen, CP; Chen, CY; Lin, CY; Shaw, SW; Wang, WS; Tzen, CY
2008-05	Prenatal diagnosis of concomitant Wolf-Hirschhorn syndrome and split hand foot malformation associated with partial monosomy 4p (4p16.1->pter) and partial trisomy 10q (10q25.1->qter)	陳持平(Chih-Ping Chen); (Yann-Jang Chen); (Schu-Rern Chern); 蔡輔仁(Fuu-Jen Tsai); (Tung-Yao Chang); (Chen-Chi Lee); (Dai-Dyi Town); (Meng-Shan Lee); (Wayseen Wang)
2007-09	Prenatal diagnosis of Dandy-Walker malformation associated with distal limb deficiencies	陳持平(Chih-Ping Chen)*
2013-12	Prenatal diagnosis of de novo cryptic microdeletions involving 5q23.1-q23.3 and 18q12.1-q12.3 by array CGH using uncultured amniocytes in a pregnancy with fetal interrupted aortic arch and atrial septal defect	陳持平(Chih-Ping Chen); (Ming-Chao Huang); (Yi-Yung Chen); (Schu-Rern Chern); (Peih-Shan Wu); (Yu-Ting Chen); (Jun-Wei Su); (Wayseen Wang)*
2005	Prenatal diagnosis of de novo partial trisomy 13q (13q22 -> qter) and partial monosomy 8p (8p23.3 -> pter) associated with holoprosencephaly, premaxillary agenesis, hexadactyly, and a hypoplastic left heart	Chen, CP; Chern, SR; Hsu, CY; Lee, CC; Lee, MS; Wang, WS
2005	Prenatal diagnosis of de novo proximal interstitial deletion of 9q and review of the literature of uncommon aneuploidies associated with increased nuchal translucency	Chen, CP; Chern, SR; Chang, TY; Chen, WL; Chen, LF; Wang, WS; Chen, HEC
2006	Prenatal diagnosis of de novo t(2;18;14) (q33.1;q12.2; q31.2),dup(5)(q34q34), del(7)(p21.1p21.1), and del(10) (q25.3q25.3) and a review of the prenatally ascertained de novo apparently balanced complex and multiple chromosomal rearrangements	陳持平(Chen CP,); (Chern SR,); (Lee CC,); 林齊強(Lin CC,); 李月君(Li YC,); 謝麗嬌(Hsieh LJ,); (Chen WL,); (Wang W.)
2011-09	Prenatal diagnosis of directly transmitted benign 4q12-q13.1 quadruplication associated with tandem segmental amplifications of the LPHN3 gene	陳持平(Chih-Ping Chen); (Yi-Ning Su); (Yu-Ting Chen); (Wen-Lin Chen); (Lee James Hsu); (Wayseen Wang)*
2007-10	Prenatal diagnosis of Fryns syndrome associated with a microdeletion at 8p23.1	陳持平(Chih-Ping Chen)*
2014-03	Prenatal diagnosis of hypomethylation at KvDMR1 and Beckwith-Wiedemann syndrome in a pregnancy conceived by ICSI and IVF-ET	陳持平(Chih-Ping Chen); (Yi-Ning Su); (Shee-Uan Chen); (Tung-Yao Chang); (Pei-Chen Wu); (Schu-Rern Chern); (Peih-Shan Wu); (Yu-Ling Kuo); (Wayseen Wang)*
2011-09	Prenatal diagnosis of limb-body wall complex with craniofacial defects	陳持平(Chih-Ping Chen); (Yi-Yung Chen); (Jun-Wei Su); (Wayseen Wang)*
2005	Prenatal diagnosis of low-level mosaic trisomy 7 by amniocentesis	Chen, CP; Chern, SR; Chen, LF; Chen, WL; Wang, W
2006	Prenatal diagnosis of low-level mosaicism for a small XIST-negative supernumerary ring X chromosome in a nondysmorphic male fetus.	陳持平(Chen CP,); (Lin SP,); 林齊強(Lin CC,); 李月君(Li YC,); 謝麗嬌(Hsieh LJ,); (Chern SR,); (Lee CC,); (Chen LF,); (Wang W.)
2011-09	Prenatal diagnosis of microvillus inclusion disease	陳持平(Chih-Ping Chen); (Yi-Ning Su); (Schu-Rern Chern); (Pei-Chen Wu); (Wayseen Wang)*
2009-12	Prenatal diagnosis of monosomy 17p (17p13.3->pter) associated with polyhydramnios, intrauterine growth restriction, ventriculomegaly and Miller-Dieker lissencephaly syndrome in a fetus	(Chin-Yi Lin); 陳持平(Chih-Ping Chen); (Chiung-Ling Liau); (Pen-Hua Su); (Teng-Fu Tsao); (Tung-Yao Chang); (Wayseen Wang)*
2008-09	Prenatal diagnosis of mosaic 1q31.3q32.1 trisomy associated with occipital encephalocele.	陳持平(Chih-Ping Chen); (Yann-Jang Chen); (Schu-Rern Chern); 蔡輔仁(Fuu-Jen Tsai); (Hung-Hung Lin); (Chen-Chi Lee); (Wayseen Wang)*

顯示項目1426-1450 / 3217. (共129頁)
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