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Taiwan Academic Institutional Repository >
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"wang wayseen"
Showing items 106-130 of 201 (9 Page(s) Totally)
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| 亞洲大學 |
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
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陳持平;Chen, Chih-Ping;Li, Shuan-Pei;Lin, Shuan-Pei;Su, Yi-Ning;Su, Yi-Ning;Ch, Schu-Rern;Chern, Schu-Rern;Su, Jun-Wei;Su, Jun-Wei;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
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
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陳持平;Chen, Chih-Ping;Su, Yi-Ning;Su, Yi-Ning;Li, Shuan-Pei;Lin, Shuan-Pei;Ch, Schu-Rern;Chern, Schu-Rern;Su, Jun-Wei;Su, Jun-Wei;Chen, Yu-Ting;Chen, Yu-Ting;Le, Meng-Shan;Lee, Meng-Shan;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
2013-03 |
Prenatal diagnosis of recurrent autosomal dominant osteogenesis imperfecta associated with unaffected parents and paternal gonadal mosaicism
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陳持平;Chen, Chih-Ping;Li, Shuan-Pei;Lin, Shuan-Pei;Su, Yi-Ning;Su, Yi-Ning;Ch, Schu-Rern;Chern, Schu-Rern;Su, Jun-Wei;Su, Jun-Wei;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
2013-01 |
Array comparative genomic hybridization characterization of prenatally detected de novo apparently balanced reciprocal translocations with or without genomic imbalance in other chromosome
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陳持平;Chen, Chih-Ping;Chen, Ming;Chen, Ming;Ma, Gwo-Chin;Ma, Gwo-Chin;Su, Yi-Ning;Su, Yi-Ning;Tsang-Ming, K;Ko, Tsang-Ming;Lin, Yi-Hui;Lin, Yi-Hui;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
2012-09 |
Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 2
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陳持平;Chen, Chih-Ping;Jun-Wei Su, ;Alan Hwa-Ruey Hsieh, ;Hsieh, Alex Hwa-Jiun;Wang, Wayseen |
| 亞洲大學 |
2012-09 |
Rapid positive confirmation of mosaicism for a small supernumerary marker chromosome as r(8) by interphase FISH, QF-PCR and aCGH on uncultured amniocytes in a pregnancy with fetal pyelectasis
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陳持平;Chen, Chih-Ping;Chen-Wen Pan, ;Wang, Wayseen |
| 亞洲大學 |
2012-09 |
Rapid positive confirmation of trisomy 21 mosaicism at amniocentesis by interphase FISH, QF-PCR and aCGH on uncultured amniocytes
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陳持平;Chen, Chih-Ping;Dai-Dyi Town, ;Wen-Lin Chen, ;Chen, Li-Feng;Meng-Shan Lee, ;Pan, Chen-Wen;Wang, Wayseen |
| 亞洲大學 |
2012-06 |
Inv dup del(10q): Identification by fluorescence in situ hybridization and array comparative genomic hybridization in a fetus with two concurrent chromosomal rearrangements
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陳持平;Chen, Chih-Ping;Jun-Wei Su, ;Chen-Chi Lee, ;Town, Dai-Dyi;Wang, Wayseen |
| 亞洲大學 |
2012-03 |
Unexplained shortening of the long bones in the third trimester as the only prenatal feature in a male fetus with 45,X/46,X,r(Y) mosaicism
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陳持平;Chen, Chih-Ping;Yu-Ting Chen, ;Chen, Li-Feng;Wang, Wayseen |
| 亞洲大學 |
2011-12 |
A de novo duplication of chromosome 21q22.11->qter associated with Down syndrome: prenatal diagnosis, molecular cytogenetic characterization and fetal ultrasound findings
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陳持平;Chen, Chih-Ping;Wang, Wayseen |
| 亞洲大學 |
2011-09 |
Chromosome 15q overgrowth syndrome: prenatal diagnosis, molecular cytogenetic characterization and perinatal findings in a fetus with dup(15)(q26.2q26.3)
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陳持平;Chen, Chih-Ping;Li-Feng Chen, ;Adam Hwa-Ming Hsieh, ;Wang, Wayseen |
| 亞洲大學 |
2011-09 |
Mosaic supernumerary r(1)(p13.2q23.3) in a 10-year-old girl with epilepsy, facial asymmetry, psychomotor retardation, kyphoscoliosis, dermatofibrosarcoma and multiple exostoses
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陳持平;Chen, Chih-Ping;Chen-Chi Lee, ;Wang, Wayseen |
| 亞洲大學 |
2011-06 |
Cytogenetic discrepancy between uncultured amniocytes and cultured amniocytes in mosaic isochromosome 20q detected at amniocentesis
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陳持平;Chen, Chih-Ping;Chen-Chi Lee, ;Wen-Lin Chen, ;Wang, Wayseen |
| 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
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陳持平;Chen, Chih-Ping;Yi-Yung Chen, ;Wang, Wayseen |
| 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
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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
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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
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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
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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 |
Balanced reciprocal translocations at amniocentesis
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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
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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
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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
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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
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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
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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
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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 |
Showing items 106-130 of 201 (9 Page(s) Totally)
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View [10|25|50] records per page
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