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Items for Author "Schu-Rern Ch"
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Showing 16 items.
Collection
Date
Title
Authors
Bitstream
[生物科技學系] 期刊論文
2017-08
Molecular cytogenetic characterization of a duplication of 15q24.2-q26.2 associated with anencephaly and neural tube defect
陳持平
;
Chih-Ping Chen
;
Chen-Yu Chen
;
Schu-Rern Ch
;
Schu-Rern Chern
;
Peih-Shan Wu
;
Shin-Wen Che
;
Shin-Wen Chen
;
Shih-Ting La
;
Shih-Ting Lai
;
Chen-Chi Lee
;
Chien-Wen Ya
;
Chien-Wen Yang
;
Wayseen Wang
[生物科技學系] 期刊論文
2017-08
Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 16
陳持平
;
Chih-Ping Chen
;
Tsang-Ming K
;
Tsang-Ming Ko
;
Schu-Rern Ch
;
Schu-Rern Chern
;
Shin-Wen Che
;
Shin-Wen Chen
;
Shih-Ting La
;
Shih-Ting Lai
;
Peih-Shan Wu
;
Chien-Wen Ya
;
Chien-Wen Yang
;
Chen-Wen Pan
;
Wayseen Wang
[生物科技學系] 期刊論文
2017-08
Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 21q11.2-q21.1 and a literature review
陳持平
;
Chih-Ping Chen
;
Ming Chen
;
Chia-Hsun Wu
;
Chen-Ju Lin
;
Schu-Rern Ch
;
Schu-Rern Chern
;
Peih-Shan Wu
;
Yen-Ni Chen
;
Shin-Wen Che
;
Shin-Wen Chen
;
Shun-Ping Ch
;
Shun-Ping Chang
;
Li-Feng Chen
;
Wayseen Wang
[生物科技學系] 期刊論文
2017-08
Prenatal diagnosis of mosaicism for trisomy 2 in a single colony at amniocentesis in a pregnancy with a favorable outcome
陳持平
;
Chih-Ping Chen
;
Jian-Pei Hua
;
Jian-Pei Huang
;
Schu-Rern Ch
;
Schu-Rern Chern
;
Shin-Wen Che
;
Shin-Wen Chen
;
Shih-Ting La
;
Shih-Ting Lai
;
Peih-Shan Wu
;
Chen-Chi Lee
;
Chien-Wen Ya
;
Chien-Wen Yang
;
Wayseen Wang
[生物科技學系] 期刊論文
2017-08
Detection of paternal uniparental disomy 9 in a neonate with prenatally detected mosaicism for a small supernumerary marker chromosome 9 and a supernumerary ring chromosome 9
陳持平
;
Chih-Ping Chen
;
Ming Chen
;
Liang-Kai Wa
;
Liang-Kai Wang
;
Schu-Rern Ch
;
Schu-Rern Chern
;
Peih-Shan Wu
;
Shin-Wen Che
;
Shin-Wen Chen
;
Shih-Ting La
;
Shih-Ting Lai
;
Shun-Ping Ch
;
Shun-Ping Chang
;
Chien-Wen Ya
;
Chien-Wen Yang
;
Chen-Wen Pan
;
Wayseen Wang
[生物科技學系] 期刊論文
2017-06
Molecular genetic characterization of a prenatally detected de novo interstitial deletion of chromosome 20p ;20p12-p13 encompassing JAG1 and a literature review of prenatal diagnosis of Alagille syndrome
陳持平
;
Chih-Ping Chen
;
Chang-Sheng
;
Chang-Sheng Yin
;
Liang-Kai Wa
;
Liang-Kai Wang
;
Schu-Rern Ch
;
Schu-Rern Chern
;
Shin-Wen Che
;
Shin-Wen Chen
;
Shih-Ting La
;
Shih-Ting Lai
;
Peih-Shan Wu
;
Wen-Lin Chen
;
Wayseen Wang
[生物科技學系] 期刊論文
2017-06
Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 11
陳持平
;
Chih-Ping Chen
;
Ming Chen
;
Pu-Tsui Wang
;
Schu-Rern Ch
;
Schu-Rern Chern
;
Shin-Wen Che
;
Shin-Wen Chen
;
Shih-Ting La
;
Shih-Ting Lai
;
Peih-Shan Wu
;
Shun-Ping Ch
;
Shun-Ping Chang
;
Chen-Wen Pan
;
Wayseen Wang
[生物科技學系] 期刊論文
2017-06
Molecular genetic characterization of a prenatally detected de novo interstitial deletion of chromosome 2q ;2q31.1-q32.1 encompassing HOXD13, ZNF385B and ZNF804A associated with syndactyly and increased first-trimester nuchal translucency
陳持平
;
Chih-Ping Chen
;
Chen-Ju Lin
;
Yen-Ni Chen
;
Schu-Rern Ch
;
Schu-Rern Chern
;
Shin-Wen Che
;
Shin-Wen Chen
;
Shih-Ting La
;
Shih-Ting Lai
;
Peih-Shan Wu
;
Li-Feng Chen
;
Wayseen Wang
[生物科技學系] 期刊論文
2017-06
Pfeiffer syndrome with FGFR2 C342R mutation presenting extreme proptosis, craniosynostosis, hearing loss, ventriculomegaly, broad great toes and thumbs, maxillary hypoplasia, and laryngomalacia
陳持平
;
Chih-Ping Chen
;
Shuan-Pei Li
;
Shuan-Pei Lin
;
Yu-Peng Liu
;
Schu-Rern Ch
;
Schu-Rern Chern
;
Shin-Wen Che
;
Shin-Wen Chen
;
Shih-Ting La
;
Shih-Ting Lai
;
Wayseen Wang
[生物科技學系] 期刊論文
2017-06
Molecular genetic characterization of a prenatally detected 1.484-Mb Xq13.3-q21.1 duplication encompassing ATRX and a literature review of syndromic intellectual disability and congenital abnormalities in males with a duplication at Xq13.3-q21.1
陳持平
;
Chih-Ping Chen
;
Hoi-Kin Yip
;
Liang-Kai Wa
;
Liang-Kai Wang
;
Schu-Rern Ch
;
Schu-Rern Chern
;
Shin-Wen Che
;
Shin-Wen Chen
;
Shih-Ting La
;
Shih-Ting Lai
;
Peih-Shan Wu
;
Wayseen Wang
[生物科技學系] 期刊論文
2017-04
Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 2
陳持平
;
Chih-Ping Chen
;
Ming Chen
;
Shun-Ping Ch
;
Shun-Ping Chang
;
Fang-Yu Hung
;
Meng-Ju Lee
;
Schu-Rern Ch
;
Schu-Rern Chern
;
Peih-Shan Wu
;
Yen-Ni Chen
;
Shin-Wen Chen
;
Chen-Chi Lee
;
Dai-Dyi Town
;
Meng-Shan Le
;
Meng-Shan Lee
;
Wen-Lin Chen
;
Wayseen Wang
[生物科技學系] 期刊論文
2017-04
Detection of mosaic 15q11.1-q11.2 deletion encompassing NBEAP1 and POTEB in a fetus with diffuse lymphangiomatosis
陳持平
;
Chih-Ping Chen
;
Kuo-Gon Wang
;
Hsu-Kuang Hu
;
Hsu-Kuang Huang
;
Cheng-Ran Pe
;
Cheng-Ran Peng
;
Schu-Rern Ch
;
Schu-Rern Chern
;
Peih-Shan Wu
;
Yen-Ni Chen
;
Shin-Wen Che
;
Shin-Wen Chen
;
Chen-Chi Lee
;
Wayseen Wang
[生物科技學系] 期刊論文
2017-04
Prenatal diagnosis and molecular cytogenetic characterization of low-level mosaic trisomy 12 at amniocentesis associated with a favorable pregnancy outcome
陳持平
;
Chih-Ping Chen
;
Chen-Ju Lin
;
Schu-Rern Ch
;
Schu-Rern Chern
;
Peih-Shan Wu
;
Yen-Ni Chen
;
Shin-Wen Che
;
Shin-Wen Chen
;
Chen-Wen Pan
;
Chien-Wen Ya
;
Chien-Wen Yang
;
Wayseen Wang
[生物科技學系] 期刊論文
2017-04
Molecular cytogenetic characterization and prenatal diagnosis of familial Xp22.33 microdeletion encompassing short stature homeobox gene in a male fetus with a favorable outcome
陳持平
;
Chih-Ping Chen
;
Tsang-Ming K
;
Tsang-Ming Ko
;
Liang-Kai Wa
;
Liang-Kai Wang
;
Shuan-Pei Li
;
Shuan-Pei Lin
;
Schu-Rern Ch
;
Schu-Rern Chern
;
Peih-Shan Wu
;
Yen-Ni Chen
;
Shin-Wen Che
;
Shin-Wen Chen
;
Meng-Shan Le
;
Meng-Shan Lee
;
Wayseen Wang
[生物科技學系] 期刊論文
2017-04
Prenatal diagnosis of mosaicism for trisomy 15 in a single colony at amniocentesis with a favorable fetal outcome
陳持平
;
Chih-Ping Chen
;
Fang-Yu Hung
;
Schu-Rern Ch
;
Schu-Rern Chern
;
Peih-Shan Wu
;
Yen-Ni Chen
;
Shin-Wen Che
;
Shin-Wen Chen
;
Chien-Wen Ya
;
Chien-Wen Yang
;
Wen-Lin Chen
;
Wayseen Wang
[生物科技學系] 期刊論文
2017-04
Prenatal diagnosis and molecular cytogenetic characterization of concomitant familial small supernumerary marker chromosome derived from chromosome 4q ;4q11.1-q13.2 and 5q13.2 microdeletion with no apparent phenotypic abnormality
陳持平
;
Chih-Ping Chen
;
Schu-Rern Ch
;
Schu-Rern Chern
;
Peih-Shan Wu
;
Peih-Shan Wu
;
Yen-Ni Chen
;
Shin-Wen Che
;
Shin-Wen Chen
;
Chien-Wen Ya
;
Chien-Wen Yang
;
Chen-Chi Lee
;
Meng-Shan Le
;
Meng-Shan Lee
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