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显示项目 81-105 / 253 (共11页)
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机构 日期 题名 作者
國立臺灣大學 2011 Maternal psychosocial factors around delivery on development of 2?year?old children: A prospective cohort study Chuang, Chao-Hua; Liao, Hua-Fang; Hsieh, Wu-Shiun; Jeng, Suh-Fang; Su, Yi-Ning; Chen, Pau-Chung
國立臺灣大學 2011 In Utero Exposure to Neurotoxic Metals and Neurodevelopment at 2 Years of Age Chen, Yu-Chuan; Liao, Hua-Fang; Hwang, Yaw-Huei; Hsieh, Wu-Shiun; Jeng, Suh-Fang; Su, Yi-Ning; Chen, Pau-Chung
國立臺灣大學 2011 The Association Between Perfluoroalkyl Chemical Levels in Umbilical Cord Blood and Neurodevelopment at 2 Years of Age Chen, Mei-Huei; Liao, Hua-Fang; Hsieh, Wu-Shiun; Jeng, Suh-Fang; Su, Yi-Ning; Wen, Ting-Wen; Lien, Guang-Wen; Chen, Chia-Yang; Chen, Pau-Chung
國立臺灣大學 2011 The Association between Perfluoroalkyl Chemical Levels in Umbilical Cord Blood and Birth Outcomes 溫婷雯; 陳美惠; 連珖?; 謝武勳; 陳家揚; 蘇怡寧; 陳保中; WEN, TING-WEN; CHEN, MEI-HUEI; LIEN, GUANG-WEN; HSIEH, WU-SHIUN; CHEN, CHIA-YANG; SU, YI-NING; CHEN, PAU-CHUNG
國立臺灣大學 2011 Favorable Neonatal Outcomes among Immigrants in Taiwan: Evidence of Healthy Immigrant Mother Effect 謝武勳; 謝佳容; 鄭素芳; 廖華芳; 蘇怡寧; 林秀娟; 張蓓貞; 陳保中; HSIEH, WU-SHIUN; HSIEH, CHIA-JUNG; JENG, SUH-FANG; LIAO, HUA-FANG; SU, YI-NING; LIN, SHIO-JEAN; CHANG, PEI-JEN; CHEN, PAU-CHUNG
國立臺灣大學 2011 Two Cases of Lowe Syndrome Presenting as Increased Fetal Nuchal Translucency 林芯伃; 李建南; 施景中; 林佳慧; 蘇怡寧; LIN, SHIN-YU; LEE, CHIEN-NAN; SHIH, JIN-CHUNG; LIN, CHIA-HUI; SU, YI-NING
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 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 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 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 2010-09 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 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 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 2010-06 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 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 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 2010-03 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

显示项目 81-105 / 253 (共11页)
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