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"陳持平"

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Showing items 186-235 of 339  (7 Page(s) Totally)
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Institution Date Title Author
亞洲大學 2011-09 Self-injurious behavior associated with trisomy 9p (9p13.1->p24.3) 陳持平;Chen, Chih-Ping
亞洲大學 2011-09 The use of misoprostol in termination of second-trimester pregnancy 陳持平;Chen, Chih-Ping
亞洲大學 2011-08 Spatiotemporal expression of SERPINE2 in the human placenta and its role in extravillous trophoblast migration and invasion 陳持平;Chen, Chih-Ping
亞洲大學 2011-06 Cytogenetic discrepancy between uncultured amniocytes and cultured amniocytes in mosaic isochromosome 20q detected at amniocentesis 陳持平;Chen, Chih-Ping;Chen-Chi Lee, ;Wen-Lin Chen, ;Wang, Wayseen
亞洲大學 2011-06 Galloway-Mowat syndrome: prenatal ultrasound and perinatal magnetic resonance imaging findings 陳持平;Chen, Chih-Ping
亞洲大學 2011-06 Partial monosomy 13q (13q21.32->qter) and partial trisomy 8p (8p12->pter) presenting with anencephaly and increased nuchal translucency: array comparative genomic hybridization characterization 陳持平;Chen, Chih-Ping
亞洲大學 2011-06 Prenatal diagnosis and array comparative genomic hybridization characterization of a de novo interstitial deletion of chromosome 20p 陳持平;Chen, Chih-Ping;Yi-Ning Su;Schu-Rern Chern;Fuu-Jen Tsai;Pei-Chen Wu;Chen-Chi Lee;Wayseen Wang
亞洲大學 2011-06 Prenatal diagnosis and molecular cytogenetic characterization of a derivative chromosome der(18;18)(q10;q10)del(18)(q11.1q12.1)del(18)(q22.1q22.3) presenting as apparent isochromosome 18q in a fetus with holoprosencephaly 陳持平;Chen, Chih-Ping
亞洲大學 2011-06 Prenatal diagnosis and molecular cytogenetic characterization of a small marker chromosome derived from Y chromosome 陳持平;Chen, Chih-Ping
亞洲大學 2011-06 Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 4 陳持平;Chen, Chih-Ping
亞洲大學 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;Chen, Chih-Ping
亞洲大學 2011-06 Rapid aneuploidy diagnosis by array comparative genomic hybridization using uncultured amniocytes in a pregnancy with fetal nuchal edema and mild ascites 陳持平;Chen, Chih-Ping
亞洲大學 2011-03 Congenital tracheal stenosis in a boy with the 22q13.3 deletion syndrome 陳持平;Chen, Chih-Ping
亞洲大學 2011-03 Inv dup del(9p): prenatal diagnosis and molecular cytogenetic characterization by fluorescence in situ hybridization and array comparative genomic hybridization 陳持平;Chen, Chih-Ping
亞洲大學 2011-03 Pathological characterization of a malformed umbilical cord associated with body stalk anomaly 陳持平;Chen, Chih-Ping
亞洲大學 2011-03 Rapid aneuploidy diagnosis by multiplex ligation-dependent probe amplification and array comparative genomic hybridization in pregnancy with major congenital malformations 陳持平;Chen, Chih-Ping;Yi-Yung Chen, ;Wang, Wayseen
亞洲大學 2011-03 Unbalanced reciprocal translocations at amniocentesis 陳持平;Chen, Chih-Ping;Chen-Wen Pan,
國立臺灣大學 2011 Mosaic Supernumerary R(1)(P13.2q23.3) in a 10-Year-Old Girl with Epilepsy, Facial Asymmetry, Psychomotor Retardation, Kyphoscoliosis, Dermatofibrosarcoma and Multiple Exostoses 陳持平; 林炫沛; 陳明; 蘇怡寧; 陳樹人; 王道遠; 劉育朋; 蔡輔仁; 李貞?; 陳燕彰; 王偉信; CHEN, CHIH-PING; LIN, SHUAN-PEI; CHEN, MING; SU, YI-NING; CHERN, SCHU-RERN; WANG, TAO-YEUAN; LIU, YU-PENG; TSAI, FUU-JEN; LEE, CHEN-CHI; CHEN, YANN-JANG; WANG, WAYSEEN
國立臺灣大學 2011 Prenatal Diagnosis and Molecular Cytogenetic Characterization of Mosaicism for a Small Supernumerary Marker Chromosome Derived from Ring Chromosome 4 陳持平; 陳明; 蘇怡寧; 蔡輔仁; 陳樹人; 吳佩臻; 陳麗鳳; 王偉信; CHEN, CHIH-PING; CHEN, MING; SU, YI-NING; TSAI, FUU-JEN; CHERN, SCHU-RERN; WU, PEI-CHEN; CHEN, LI-FENG; WANG, WAYSEEN
國立臺灣大學 2011 Prenatal Diagnosis of Mosaic Trisomy 8: Clinical Report and Literature Review 陳持平; 陳明; 潘怡如; 蘇怡寧; 陳樹人; 蔡輔仁; 王偉信; CHEN, CHIH-PING; CHEN, MING; PAN, YI-JU; SU, YI-NING; CHERN, SCHU-RERN; TSAI, FUU-JEN; WANG, WAYSEEN
亞洲大學 2010-12 A 5.3-Mb duplication of 9p12->p13.1 characterized by array CGH in a female infant with developmental delay 陳持平;Chen, Chih-Ping;Lin, Shuan-Pei;Chern, Schu-Rern;Tsai, Fuu-Jen;Lee, Chen-Chi;Pan, Chen-Wen;Wu, Pei-Chen;Wang, Wayseen
亞洲大學 2010-12 Alzheimer's Disease: Aging, Insomnia and Epigenetics ;Wu, Tzong-Yuan;陳持平;Chen, Chih-Ping;Jinn, Tzyy-Rong
亞洲大學 2010-12 Balanced reciprocal translocations at amniocentesis 陳持平;Chen, Chih-Ping;Wu, Pei-Chen;Su, Yi-Ning;Chern, Schu-Rern;Tsai, Fuu-Jen;Lee, Chen-Chi;Town, Dai-Dyi;Chen, Wen-Lin;Chen, Li-Feng;Pan, Chen-Wen;Wang, Wayseen
亞洲大學 2010-12 Chromosome 1p36 deletion syndrome: prenatal diagnosis, molecular cytogenetic characterization and fetal ultrasound findings 陳持平;Chen, Chih-Ping;Chen, Ming;Su, Yi-Ning;Hsu, Chin-Yuan;Tsai, Fuu-Jen;Chern, Schu-Rern;Wu, Pei-Chen;Lee, Chen-Chi;Wang, Wayseen
亞洲大學 2010-12 Microvillus inclusion disease: prenatal ultrasound findings, molecular diagnosis and genetic counseling of congenital diarrhea 陳持平;Chen, Chih-Ping;Chiang, Ming-Chou;Wang, Tzu-Hao;Hsueh, Chuen;Chang, Shueen-Dyh;Tsai, Fuu-Jen;Wang, Chao-Ning;Chern, Schu-Rern;Wang, Wayseen
亞洲大學 2010-12 Partial trisomy 10q (10q25.1->qter) and partial monosomy 13q (13q34->qter) presenting with fetal pyelectasis: prenatal diagnosis and array comparative genomic hybridization characterization 陳持平;Chen, Chih-Ping;Su, Yi-Ning;Tsai, Fuu-Jen;Hsu, Chin-Yuan;Chern, Schu-Rern;Wu, Pei-Chen;Lee, Chen-Chi;Chen, Wen-Lin;Wang, Wayseen
亞洲大學 2010-12 Partial trisomy 16p (16p12.2->pter) and partial monosomy 22q (22q13.31->qter) presenting with fetal ascites and ventriculomegaly: prenatal diagnosis and array comparative genomic hybridization characterization 陳持平;Chen, Chih-Ping;Su, Yi-Ning;Young, Richard Shih-Hung;Tsai, Fuu-Jen;Wu, Pei-Chen;Chern, Schu-Rern;Town, Dai-Dyi;Pan, Chen-Wen;Wang, Wayseen
亞洲大學 2010-12 Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 8 陳持平;Chen, Chih-Ping;Chen, Ming;Ko, Tsang-Ming;Ma, Gwo-Chin;Tsai, Fuu-Jen;Tsai, Ming-Song;Wu, Pei-Chen;Lee, Chen-Chi;Che, Li-Feng;Wang, Wayseen
亞洲大學 2010-12 Prenatal diagnosis of partial monosomy 1q (1q42.3->qter) associated with hydrocephalus and corpus callosum agenesis 陳持平;Chen, Chih-Ping;Chern, Schu-Rern;Tsai, Fuu-Jen;Lin, Hung-Hung;Wu, Pei-Chen;Lee, Chen-Chi;Pan, Chen-Wen;Wang, Wayseen
亞洲大學 2010-12 Prenatal sonographic features of Miller-Dieker syndrome 陳持平;Chen, Chih-Ping
亞洲大學 2010-12 Recurrent distal 16q duplication and terminal 22q deletion: prenatal diagnosis and genetic counseling 陳持平;Chen, Chih-Ping;Huang, Ming-Chao;Su, Yi-Ning;Tsai, Fuu-Jen;Wu, Pei-Chen;Lee, Chen-Chi;Town, Dai-Dyi;Pan, Chen-Wen;Wang, Wayseen
亞洲大學 2010-12 Stroke during pregnancy and puerperium: clinical perspectives ;Cheng, Shih-Jung;Chen, Pei-Hao;Chen, Lu-An;陳持平;Chen, Chih-Ping
亞洲大學 2010-09 A de novo 7.9 Mb deletion in 22q13.2->qter in a boy with autistic features, epilepsy, developmental delay atopic dermatitis and abnormal immunological findings 陳持平;Chen, Chih-Ping;Lin, Shuan-Pei;Chern, Schu-Rern;Tsai, Fuu-Jen;Wu, Pei-Chen;Lee, Chen-Chi;Chen, Yu-Ting;Wang, Wayseen
亞洲大學 2010-09 Mosaic ring chromosome 18, ring chromosome 18 duplication/deletion and disomy 18: perinatal findings and molecular cytogenetic characterization by fluorescence in situ hybridization and array comparative genomic hybridization 陳持平;Chen, Chih-Ping;Guo, Yung-Ting;Lin, Shuan-Pei;Su, Yi-Ning;Chen, Yann-Jang;Hseuh, Rui-Yuan;Lin, Yi-Hui;Wu, Pei-Chen;Lee, Chen-Chi;Chen, Yu-Ting;Wang, Wayseen
亞洲大學 2010-09 Mosaic trisomy 7 at amniocentesis: prenatal diagnosis and molecular genetic analyses 陳持平;Chen, Chih-Ping;Su, Yi-Ning;Chern, Schu-Rern;Hwu, Yu-Ming;Lin, Shuan-Pei;Hsu, Chyong-Hsin;Tsai, Fuu-Jen;Wang, Tao-Yeuan;Wu, Pei-Chen;Lee, Chen-Chi;Chen, Yu-Ting;Chen, Li-Feng;Wang, Wayseen
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

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