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"陳持平"的相关文件
显示项目 261-310 / 339 (共7页) << < 1 2 3 4 5 6 7 > >> 每页显示[10|25|50]项目
| 國立臺灣大學 |
2010 |
Second-Trimester Molecular Prenatal Diagnosis of Sporadic Apert Syndrome Following Sonographic Findings of Mild Ventriculomegaly and Clenched Hands Mimicking Trisomy 18
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陳持平; 蘇怡寧; 徐金源; 蔡輔仁; 陳樹人; 吳佩臻; 王偉信; 林珮瑩; CHEN, CHIH-PING; SU, YI-NING; HSU, CHIN-YUAN; TSAI, FUU-JEN; CHERN, SCHU-RERN; WU, PEI-CHEN; WANG, WAYSEEN; LING, PEI-YING |
| 國立臺灣大學 |
2010 |
Second-Trimester Maternal Serum Quadruple Test for down Syndrome Screening : A Taiwanese Population-Based Study
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蕭勝文; 林芯伃; 林佳慧; 蘇怡寧; 鄭博仁; 李建南; 陳持平; SHAW, SHENG-WEN; LIN, SHIN-YU; LIN, CHIA-HUI; SU, YI-NING; CHENG, PO-JEN; LEE, CHIEN-NAN; CHEN, CHIH-PING |
| 國立臺灣大學 |
2010 |
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
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陳持平; 陳明; 蘇怡寧; 蔡輔仁; 陳樹人; 徐金源; 吳佩臻; 李東杰; 馬國欽; 王偉信; CHEN, CHIH-PING; CHEN, MING; SU, YI-NING; TSAI, FUU-JEN; CHERN, SCHU-RERN; HSU, CHIN-YUAN; WU, PEI-CHEN; LEE, DONG-JAY; MA, GWO-CHIN; WANG, WAYSEEN |
| 國立臺灣大學 |
2010 |
Chromosome 1p36 Deletion Syndrome: Prenatal Diagnosis, Molecular Cytogenetic Characterization and Fetal Ultrasound Findings
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陳持平; 陳明; 蘇怡寧; 徐金源; 蔡輔仁; 陳樹人; 吳佩臻; 李貞?; CHEN, CHIH-PING; CHEN, MING; SU, YI-NING; HSU, CHIN-YUAN; TSAI, FUU-JEN; CHERN, SCHU-RERN; WU, PEI-CHEN; LEE, CHEN-CHI |
| 亞洲大學 |
2009-12 |
Down syndrome due to unbalanced homologous acrocentric rearrangements and its recurrence in subsequent pregnancies: prenatal diagnosis by amniocentesis
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陳持平;Chen, Chih-Ping;Chern, Schu-Rern;Tsai, Fuu-Jen;Wu, Pei-Chen;Lee, Chen-Chi;Chiang, Shu-Shien;Wang, Wayseen |
| 亞洲大學 |
2009-12 |
Limb-body wall complex in one fetus of a dizygotic twin pregnancy obtained by egg donation, in vitro fertilization and embryo transfer: prenatal diagnosis and literature review
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陳持平;Chen, Chih-Ping;Lee, Maw-Shuan;Tsai, Fuu-Jen;Huang, Ming-Chao;Chern, Schu-Rern;Wang, Wayseen |
| 亞洲大學 |
2009-12 |
Prenatal diagnosis of a 22q11.2 microdeletion in a fetus with double-outlet right ventricle, pulmonary stenosis and a ventricular septal defect by array comparative genomic hybridization
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陳持平;Chen, Chih-Ping;Su, Yi-Ning;Chang, Tung-Yao;Chern, Schu-Rern;Tsai, Fuu-Jen;Hwang, Jonathan Kwei;Wang, Wayseen |
| 亞洲大學 |
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
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;Lin, Chin-Yi;陳持平;Chen, Chih-Ping;Liau, Chiung-Ling;Su, Pen-Hua;Tsao, Teng-Fu;Chang, Tung-Yao;Wang, Wayseen |
| 亞洲大學 |
2009-12 |
Prenatal diagnosis of terminal 2q deletion and distal 15q duplication by array comparative genomic hybridization using uncultured amniocytes
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陳持平;Chen, Chih-Ping;Su, Yi-Ning;Tsai, Fuu-Jen;Lin, Hung-Hung;Chern, Schu-Rern;Lee, Meng-Shan;Hwang, Jonathan Kwei;Chen, Teresa Hsiao-Tien;Wang, Wayseen |
| 亞洲大學 |
2009-12 |
Prenatal sonographic features of fetuses in trisomy 13 pregnancies (III)
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陳持平;Chen, Chih-Ping |
| 亞洲大學 |
2009-12 |
Trisomy 13 mosaicism associated with cyclopia and cystic hygroma
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陳持平;Chen, Chih-Ping;Chern, Schu-Rern;Tsai, Fuu-Jen;Wu, Pei-Chen;Lee, Chen-Chi;Wang, Wayseen |
| 亞洲大學 |
2009-12 |
Unbalanced and balanced acrocentric rearrangements involving chromosomes other than chromosome 21 at amniocentesis
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陳持平;Chen, Chih-Ping;Chern, Schu-Rern;Wu, Pei-Chen;Tsai, Fuu-Jen;Lee, Chen-Chi;Town, Dai-Dyi;Chen, Wen-Lin;Chen, Li-Feng;Lee, Meng-Shan;Pan, Chen-Wen;Wang, Wayseen |
| 亞洲大學 |
2009-09 |
Concomitant craniorachischisis and omphalocele in a male fetus: prenatal magnetic resonance imaging findings and literature review
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陳持平;Chen, Chih-Ping;Liu, Yu-Peng;Tsai, Fuu-Jen;Chen, Chen-Yu;Lin, Hung-Hung;Wu, Pei-Chen;Wang, Wayseen |
| 亞洲大學 |
2009-09 |
Pernatal diagnosis of partial trisomy 14q (14q31.1->qter) and partial monosomy 5p (5p13.2->pter) associated with polyhydramnios, short limbs, micropenis and brain malformations
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陳持平;Chen, Chih-Ping;Chern, Schu-Rern;F.J.Tsai;C.C.Lee;L.F.Chen;W.Wang |
| 亞洲大學 |
2009-09 |
Prenatal diagnosis and molecular analysis of triploidy in a fetus with intrauterine growth restriction, relative macrocephaly and holoprosencephaly
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陳持平;Chen, Chih-Ping;Chern, Schu-Rern;Tsai, Fuu-Jen;Hsu, Chin-Yuan;Ko, Kevin;Wang, Wayseen |
| 亞洲大學 |
2009-09 |
Prenatal diagnosis and molecular analysis of trisomy 13 mosaicism
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陳持平;Chen, Chih-Ping;Chern, Schu-Rern;Tsai, Fuu-Jen;Lin, Hung-Hung;Pan, Chen-Wen;Wang, Wayseen |
| 亞洲大學 |
2009-09 |
Prenatal magnetic resonance imaging, ultrasound imaging findings and genetic analysis of concomitant rhabdomyomas and cerebral tuberous sclerosis
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陳持平;Chen, Chih-Ping;Su, Yi-Ning;Chang, Tung-Yao;Liu, Yu-Peng;Tsai, Fuu-Jen;Hwang, Jonathan Kwei;Wang, Wayseen |
| 亞洲大學 |
2009-09 |
Prenatal sonographic features of fetuses in trisomy 13 pregnancies (I)
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陳持平;Chen, Chih-Ping |
| 亞洲大學 |
2009-09 |
Prenatal sonographic features of fetuses in trisomy 13 pregnancies (II)
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陳持平;Chen, Chih-Ping |
| 亞洲大學 |
2009-06 |
Association of Interleukin-10 A-592C Polymorphism in Taiwanese Children with Kawasaki Disease
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薛凱中;Hsueh, KC;林應如;Lin, YJ;張正成;Chang, JS;萬磊;Wan, L;蔡育勳;Tsai, YH;蔡長海;陳持平;Chen, Chih-Ping;蔡輔仁;Tsai, Fuu-Jen |
| 亞洲大學 |
2009-05 |
Prenatal sonographic features of Beckwith-Wiedemann syndrome
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陳持平;Chen, Chih-Ping |
| 亞洲大學 |
2009-03 |
PLACENTAL ABNORMALITIES AND PREECLAMPSIA IN TRISOMY 13 PREGNANCIES
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陳持平;Chen, Chih-Ping |
| 亞洲大學 |
2009-03 |
PLACENTAL ABNORMALITIES AND PREECLAMPSIA IN TRISOMY 13 PREGNANCIES
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陳持平;Chen, Chih-Ping |
| 亞洲大學 |
2009-03 |
PRENATAL DIAGNOSIS OF 46,XX,DER(13;21)(Q10;Q10),+21 AND TRANSIENT ABNORMAL MYELOPOIESIS IN A FETUS WITH HEPATOSPLENOMEGALY AND SPONTANEOUS RESOLUTION OF FETAL ASCITES
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陳持平;Chen, Chih-Ping;Tsai, Fuu-Jen;Chern, Schu-Rern;Chang, Tung-Yao;Hsu, Chin-Yuan;Lin, Hung-Hung;Wang, Wayseen |
| 亞洲大學 |
2009-02 |
PRENATAL DIAGNOSIS and GENETIC COUNSELING of NEURAL TUBE DEFECTS-An OVERVIEW and ATLAS of CASES
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陳持平;Chen, Chih-Ping |
| 亞洲大學 |
2009-01 |
A 12 Mb deletion of 6p24.1 -> pter in an 18-gestational-week fetus with orofacial clefting, the Dandy-Walker malformation and bilateral multicystic kidneys
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陳持平;Chen, Chih-Ping;Tzen, Chin-Yuan;Chern, Schu-Rern;Tsai, Fuu-Jen;Hsu, Chin-Yuan;Lee, Chen-Chi;Lee, Meng-Shan;Pan, Chen-Wen;Wang, Wayseen |
| 國立臺灣大學 |
2009 |
A Case of Restrictive Dermopathy with Complete Chorioamniotic Membrane Separation Caused by a Novel Homozygous Nonsense Mutation in the Zmpste24 Gene
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陳明; 馬國欽; 柯瑜媛; 張舜評; 陳持平; 李東杰; 李孟倫; 李美慧; 陳子和; 陳加祥; 林惠美; 劉青山; CHEN, MING; MA, GWO-CHIN; KE, YU-YUAN; CHANG, SHUN-PING; CHEN, CHIH-PING; LEE, DONG-JAY; LEE, MENG-LUEN; LEE, MEI-HUI; CHEN, TZE-HO; CHEN, CHIA-HSIANG; LIN, HUI-MEI; LIU, CHIN-SAN |
| 國立臺灣大學 |
2009 |
Mutation Spectrum of the Fibrillin-1 (Fbn1) Gene in Taiwanese Patients with Marfan Syndrome
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洪加政; 李建南; 鄭惠予; 林炫沛; 陳銘仁; 陳持平; 張千慧; 游治節; 邱馨慧; 鄭文芳; 何弘能; 牛道明; 蘇怡寧; HUNG, CHIA-CHENG; LEE, CHIEN-NAN; CHENG, HUI-YU; LIN, SHUAN-PEI; CHEN, MING-REN; CHEN, CHIH-PING; CHANG, CHIEN-HUI; YU, CHIH- CHIEH; CHIU, HSIN-HUI; CHENG, WEN-FANG; HO, HONG-NERNG; NIU, DAU-MING; SU, YI-NING |
| 國立臺灣大學 |
2009 |
Identification of Cpg Methylation of the Snrpn Gene by Methylation- Specific Multiplex Pcr
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洪加政; 林芯伃; 林炫沛; 牛道明; 李妮鍾; 鄭文芳; 陳持平; 林文澧; 李建南; 蘇怡寧; HUNG, CHIA-CHENG; LIN, SHIN-YU; LIN ,SHUAN-PEI; NIU, DAU-MING; LEE, NI-CHUNG; CHENG, WEN-FANG; CHEN, CHIH-PING; LIN, WIN-LI; LEE, CHIEN-NAN; SU, YI-NING |
| 國立臺灣大學 |
2009 |
22q11.2 Microdeletion in a Fetus with Double-Outlet Right Ventricle, Pulmonary Stenosis and a Ventricular Septal Defect: Prenatal Diagnosis by Array Comparative Genomic Hybridization
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陳持平; 蘇怡寧; 張東曜; 陳樹人; 蔡輔仁; 王偉信; CHEN, CHIH-PING; SU, YI-NING; CHANG, TUNG-YAO; CHERN, SCHU-RERN; TSAI, FUU-JEN; WANG, WAYSEEN |
| 國立臺灣大學 |
2009 |
Terminal 2q Deletion and Distal 15q Duplication: Prenatal Diagnosis by Array Comparative Genomic Hybridization Using Uncultured Amniocytes
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陳持平; 蘇怡寧; 蔡輔仁; 林虹宏; 陳樹人; 李孟珊; 王偉信; CHEN, CHIH-PING; SU, YI-NING; TSAI, FUU-JEN; LIN, HUNG-HUNG; CHERN, SCHU-RERN; LEE, MENG-SHAN; WANG, WAYSEEN |
| 國立臺灣大學 |
2009 |
Prenatal Magnetic Resonance Imaging, Ultrasound Imaging Findings and Genetic Analysis of Concomitant Rhabdomyomas and Cerebral Tuberous Sclerosis
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陳持平; 蘇怡寧; 張東曜; 劉育朋; 蔡輔仁; 王偉信; CHEN, CHIH-PING; SU, YI-NING; CHANG, TUNG-YAO; LIU, YU-PENG; TSAI, FUU-JEN; WANG, WAYSEEN |
| 國立臺灣大學 |
2009 |
Genetic Evaluation and Management of Fetal Chylothorax: Review and Insights from a Case of Noonan Syndrome
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陳加祥; 陳子和; 郭守仁; 陳持平; 李東杰; 柯瑜媛; 葉坤土; 馬國欽; 劉青山; 施景中; 陳明; CHEN, CHIA-HSIANG; CHEN, TZE-HO; KUO, SHOU-JEN; CHEN, CHIH-PING; LEE, DONG-JAY; KE, YU-YUAN; YEH, KUN-TU; MA, GWO-CHIN; LIU, CHIN-SAN; SHIH, JIN -CHUNG; CHEN, MING |
| 亞洲大學 |
2008-12 |
CONCOMITANT EXENCEPHALY AND LIMB DEFECTS ASSOCIATED WITH PENTALOGY OF CANTRELL
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陳持平;Chen, Chih-Ping;Tzen, Chin-Yuan;Chen, Chen-Yu;Tsai, Fuu-Jen;Wang, Wayseen |
| 亞洲大學 |
2008-12 |
LIMB-BODY WALL COMPLEX WITH CRANIOFACIAL DEFECTS AFTER OVARIAN STIMULATION
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陳持平;Chen, Chih-Ping;Tsai, Fuu-Jen;Chen, Chen-Yu;Lin, Hung-Hung;Wang, Wayseen |
| 亞洲大學 |
2008-10 |
Prenatal Diagnosis of Partial Trisomy 3p (3p21 -> pter) and Partial Monosomy 11q (11q23 -> qter) Associated with Abnormal Sonographic Findings of Holoprosencephaly, Orofacial Clefts, Pyelectasis and a Unilateral Duplex Renal System
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陳持平;Chen, Chih-Ping;Wang, Tzu-Hao;Lin, Chyi-Chyang;Tsai, Fuu-Jen;Hsieh, Lie-Jiau;Wang, Wayseen |
| 亞洲大學 |
2008-09 |
PRENATAL DIAGNOSIS, FETAL SURGERY, RECURRENCE RISK AND DIFFERENTIAL DIAGNOSIS OF NEURAL TUBE DEFECTS
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陳持平;Chen, Chih-Ping |
| 亞洲大學 |
2008-09 |
SYNDROMES, DISORDERS AND MATERNAL RISK FACTORS ASSOCIATED WITH NEURAL TUBE DEFECFS (V)
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陳持平;Chen, Chih-Ping |
| 亞洲大學 |
2008-09 |
SYNDROMES, DISORDERS AND MATERNAL RISK FACTORS ASSOCIATED WITH NEURAL TUBE DEFECTS (VI)
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陳持平;Chen, Chih-Ping |
| 亞洲大學 |
2008-09 |
SYNDROMES, DISORDERS AND MATERNAL RISK FACTORS ASSOCIATED WITH NEURAL TUBE DEFECTS (VII)
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陳持平;Chen, Chih-Ping |
| 亞洲大學 |
2008-06 |
SYNDROMES, DISORDERS AND MATERNAL RISK FACTORS ASSOCIATED WITH NEURAL TUBE DEFECTS (III)
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陳持平;Chen, Chih-Ping |
| 亞洲大學 |
2008-06 |
SYNDROMES, DISORDERS AND MATERNAL RISK FACTORS ASSOCIATED WITH NEURAL TUBE DEFECTS (IV)
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陳持平;Chen, Chih-Ping |
| 亞洲大學 |
2008-03 |
CONCOMITANT OMPHALOCELE AND ANENCEPHALY ASSOCIATED WITH TRISOMY 18 AND ARTHROGRYPOSIS DIAGNOSED IN EARLY PREGNANCY
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陳持平;Chen, Chih-Ping;Chang, Tung-Yao;Lin, Hung-Hung;Chern, Schu-Rern;Wang, Wayseen |
| 亞洲大學 |
2008-03 |
PRENATAL VISUALIZATION OF CEBOCEPHALY WITH A PROMINENT NOSE IN A SECOND-TRIMESTER FETUS WITH ALOBAR HOLOPROSENCEPHALY AND TRISOMY 13
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陳持平;Chen, Chih-Ping;Shih, Jin-Chung;Tzen, Chin-Yuan;Chern, Schu-Rern;Lin, Chen-Ju;Wang, Wayseen |
| 亞洲大學 |
2008-03 |
SYNDROMES, DISORDERS AND MATERNAL RISK FACTORS ASSOCIATED WITH NEURAL TUBE DEFECTS (I)
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陳持平;Chen, Chih-Ping |
| 亞洲大學 |
2008-03 |
SYNDROMES, DISORDERS AND MATERNAL RISK FACTORS ASSOCIATED WITH NEURAL TUBE DEFECTS (II)
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陳持平;Chen, Chih-Ping |
| 國立臺灣大學 |
2008 |
Genotyping of the G1138A mutation of the FGFR3 gene in patients with achondroplasia using high-resolution melting analysis
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Hung, Chia-Cheng; Lee, Chien-Nan; Chang, Chien-Hui; Jong, Yuh-Jyh; Chen, Chih-Ping; Hsieh, Wu-Shiun; Su, Yi-Ning; Lin, Win-Li; 洪加政; 李建南; 張千慧; 鐘育志; 陳持平; 謝武勳; 蘇怡寧; 林文澧 |
| 國立臺灣大學 |
2008 |
First- and Second-Trim Ester down Syndrome Screening: Current Strategies and Clinical Guidelines
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蕭勝文; 徐振傑; 李建南; 蕭慶華; 陳持平; 謝燦堂; 鄭博仁; SHAW, SHENG-WEN; HSU, JENN-J; LEE, CHIEN- NAN; HSIAO, CHING-HUA; CHEN, CHIH-PING; HSIEH, T'SANG-T'ANG; CHENG, PO-JEN |
| 國立臺灣大學 |
2008 |
Genetic Analysis of Mucopolysaccharidosis Type Vi in Taiwanese Patients
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林瑋德; 林炫沛; 王仲興; 胡務亮; 莊志光; 林秀娟; 陳持平; 蔡輔仁; LIN, WEI-DE; LIN, SHUAN-PEI; WANG, CHUNG- HSING; HWU, WUH-LIANG; CHUANG, CHIH-KUANG; LIN, SHIO-JEAN; CHEN, CHIH-PING; TSAI, FUU- JEN |
| 國立臺灣大學 |
2008 |
Craniosynostosis and Congenital Tracheal Anomalies in an Infant with Pfeiffer Syndrome Carrying the W290c Fgfr2 Mutation
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陳持平; 林炫沛; 蘇怡寧; 蔡輔仁; 王偉信; CHEN, CHIH-PING; LIN, SHUAN-PEI; SU, YI-NING; TSAI, FUU-JEN; WANG, WAYSEEN |
显示项目 261-310 / 339 (共7页) << < 1 2 3 4 5 6 7 > >> 每页显示[10|25|50]项目
|