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教育部委託研究計畫      計畫執行:國立臺灣大學圖書館
 
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機構 日期 題名 作者
亞洲大學 2010-09 Mosaic trisomy 9 at amniocentesis: prenatal diagnosis and molecular genetic analyses 陳持平;Chen, Chih-Ping;Lin, Hsien-Ming;Su, Yi-Ning;Chern, Schu-Rern;Tsai, Fuu-Jen;Wu, Pei-Chen;Lee, Chen-Chi;Chen, Yu-Ting;Lee, Meng-Shan;Pan, Chen-Wen;Wang, Wayseen
亞洲大學 2010-09 Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 21 陳持平;Chen, Chih-Ping;Lin, Chyi-Chyang;Ko, Tsang-Ming;Tsai, Fuu-Jen;Chern, Schu-Rern;Lee, Chen-Chi;Chen, Yu-Ting;Wu, Pei-Chen;Wang, Wayseen
亞洲大學 2010-09 Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 22 陳持平;Chen, Chih-Ping;Lin, Chyi-Chyang;Su, Yi-Ning;Tsai, Fuu-Jen;Chern, Schu-Rern;Lee, Chen-Chi;Chen, Wen-Ling;Chen, Li-Feng;Wu, Pei-Chen;Wang, Wayseen
亞洲大學 2010-09 Prenatal diagnosis and molecular cytogenetic characterization of de novo partial trisomy 7p (7p15.3->pter) and partial monosomy 13q (13q33.3->qter) associated with Dandy-Walker malformation, abnormal skull development and microcephaly 陳持平;Chen, Chih-Ping;Chen, Ming;Su, Yi-Ning;Tsai, Fuu-Jen;Chern, Schu-Rern;Hsu, Chin-Yuan;Wu, Pei-Chen;Town, Dai-Dyi;Lee, Dong-Jay;Ma, Gwo-Chin;Wang, Wayseen
亞洲大學 2010-09 Prenatal diagnosis of persistent cloaca with hydrometrocolpos and ascites by magnetic resonance imaging in one fetus of a dizygotic twin pregnancy 陳持平;Chen, Chih-Ping;Liu, Yu-Peng;Chang, Tung-Yao;Tsai, Fuu-Jen;Chen, Chen-Yu;Wu, Pei-Chen;Chen, Teresa Hsiao-Tien;Wang, Wayseen
亞洲大學 2010-09 Prenatal diagnosis of rhabdomyomas and cerebral tuberous sclerosis by magnetic resonance imaging in one fetus of a dizygotic twin pregnancy associated with a frameshift mutation in the TSC2 gene 陳持平;Chen, Chih-Ping;Su, Yi-Ning;Chang, Tung-Yao;Liu, Yu-Peng;Tsai, Fuu-Jen;Chen, Ming-Ren;Hwang, Jonathan Kwei;Chen, Teresa Hsiao-Tien;Wang, Wayseen
亞洲大學 2010-09 Prenatal diagnosis of satellited 21q derived from pericentric inversion involving the satellite stalk region and terminal 21q 陳持平;Chen, Chih-Ping;Tsai, Fuu-Jen;Lee, Chen-Chi;Chen, Wen-Lin;Pan, Chen-Wen;Wu, Pei-Chen;Wang, Wayseen
亞洲大學 2010-07 Array-CGH detection of a de novo 2.8 Mb deletion in 2q24.2->q24.3 in a girl with autistic features and developmental delay 陳持平;Chen, Chih-Ping;Lin, Shuan-Pei;Chern, Schu-Rern;Chen, Yann-Jang;Tsai, Fuu-Jen;Wu, Pei-Chen;Wang, Wayseen
亞洲大學 2010-06 Apert syndrome associated with upper airway obstruction and gastroesophageal reflux presenting polyhydramnios in the third trimester 陳持平;Chen, Chih-Ping;Lin, Shuan-Pei;Su, Yi-Ning;Chen, Chen-Yu;Tsai, Fuu-Jen;Liu, Yu-Peng;Chern, Schu-Rern;Wu, Pei-Chen;Chen, Hsaio-En Cindy;Wang, Wayseen
亞洲大學 2010-06 Deletion 2q37.3->qter and duplication 15q24.3->qter characterized by array CGH in a girl with epilepsy and dysmorphic features 陳持平;Chen, Chih-Ping;Lin, Shuan-Pei;Chern, Schu-Rern;Tsai, Fuu-Jen;Wu, Pei-Chen;Lee, Chen-Chi;Chen, Li-Feng;Lee, Meng-Shan;Wang, Wayseen
亞洲大學 2010-06 Detection and comparison of the levels of cytomegalovirus DNA in amniotic fluid and fetal ascites in a second-trimester fetus with massive ascites, hyperechogenic bowel, ventriculomegaly and intrauterine growth restriction 陳持平;Chen, Chih-Ping;Chern, Schu-Rern;Wang, Tao-Yeuan;Tsai, Fuu-Jen;Lin, Hung-Hung;Wu, Pei-Chen;Wang, Wayseen
亞洲大學 2010-06 Detection of a balanced homologous acrocentric rearrangement rea(14q14q) and low-grade X-chromosome mosaicism in a couple with repeated pregnancy losses 陳持平;Chen, Chih-Ping;Chern, Schu-Rern;Wu, Chia-Hsun;Tsai, Fuu-Jen;Wu, Pei-Chen;Wang, Wayseen
亞洲大學 2010-06 Epicatechin gallate decreases the viability and subsequent embryonic development of mouse blastocysts Tu, Hsiao-Chen;陳持平;Chen, Chih-Ping;Chan, Wen-Hsiung
亞洲大學 2010-06 Fetal magnetic resonance imaging demonstration of central nervous system abnormalities and polydactyly associated with Joubert syndrome 陳持平;Chen, Chih-Ping;Su, Yi-Ning;Huang, Jon-Kway;Liu, Yu-Peng;Tsai, Fuu-Jen;Yang, Chun-Kuang;Huang, Jian-Pei;Chen, Chen-Yu;Wu, Pei-Chen;Wang, Wayseen
亞洲大學 2010-06 Mosaic tetrasomy 12p with discrepancy between fetal tissues and extraembryonic tissues: molecular analysis and possible mechanism of formation 陳持平;Chen, Chih-Ping;Su, Yi-Ning;Chern, Schu-Rern;Tsai, Fuu-Jen;Wu, Pei-Chen;Chen, Hsaio-En Cindy;Chiang, Shu-Shien;Wang, Wayseen
亞洲大學 2010-06 Pathophysiology of increased fetal nuchal translucency thickness 陳持平;Chen, Chih-Ping
亞洲大學 2010-06 Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 18 and associated with a reciprocal translocation involving chromosomes 17 and 18 陳持平;Chen, Chih-Ping;Lin, Chyi-Chyang;Su, Yi-Ning;Tsai, Fuu-Jen;Chen, Yu-Ting;Chern, Schu-Rern;Lee, Chen-Chi;Town, Dai-Dyi;Chen, Li-Feng;Wu, Pei-Chen;Wang, Wayseen
亞洲大學 2010-06 Prenatal sonographic features of Pallister-Killian syndrome 陳持平;Chen, Chih-Ping
亞洲大學 2010-03 Abnormally flat facial profile on two- and three-dimensional ultrasound and array comparative genomic hybridization for the diagnosis of Pallister-Killian syndrome 陳持平;Chen, Chih-Ping;Su, Yi-Ning;Hsu, Chin-Yuan;Tsai, Fuu-Jen;Chien, Shu-Chin;Chern, Schu-Rern;Lee, Meng-Shan;Wu, Pei-Chen;Chen, Hsaio-En Cindy;Wang, Wayseen
亞洲大學 2010-03 Prenatal diagnosis and genetic counseling of mosaic trisomy 13 陳持平;Chen, Chih-Ping
亞洲大學 2010-03 Prenatal diagnosis of a 4.9-Mb deletion of 10q11.21->q11.23 by array comparative genomic hybridization 陳持平;Chen, Chih-Ping;Su, Yi-Ning;Chern, Schu-Rern;Tsai, Fuu-Jen;Hsu, Chin-Yuan;Lee, Chen-Chi;Wang, Wayseen
亞洲大學 2010-03 Prenatal sonographic features of the fetuses in trisomy 13 pregnancies (IV) 陳持平;Chen, Chih-Ping
亞洲大學 2010-03 Rapid genome-wide aneuploidy diagnosis using uncultured amniocytes and array CGH in pregnancy with abnormal ultrasound findings detected in late second and third trimesters 陳持平;Chen, Chih-Ping;Su, Yi-Ning;Tsai, Fuu-Jen;Chern, Schu-Rern;Hsu, Chin-Yuan;Huang, Ming-Chao;Wang, Wayseen
亞洲大學 2010-03 Resectoscopic excision of the vaginal septum in a virgin with uterus didelphys and obstructed unilateral vagina ;Shih, Chao-Lan;Hung, Yao-Ching;陳持平;Chen, Chih-Ping;Chien, Shu-Chin;Lin, Wu-Chou
亞洲大學 2010-03 Second-trimester molecular prenatal diagnosis of sporadic Apert syndrome following sonographic findings of mild ventriculomegaly and clenched hands mimicking trisomy 18 陳持平;Chen, Chih-Ping;Su, Yi-Ning;Hsu, Chin-Yuan;Ling, Pei-Ying;Tsai, Fuu-Jen;Chern, Schu-Rern;Wu, Pei-Chen;Chen, Hsaio-En Cindy;Wang, Wayseen

顯示項目 221-245 / 339 (共14頁)
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