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Prenatal diagnosis and array comparative genomic hybridization characterization of trisomy 21 in a fetus associated with right congenital diaphragmatic hernia and a review of the literature of chromosomal abnormalities associated with congenital diaphragmatic hernia

机译：产前诊断和阵列比较基因组杂交表征胎儿21三体与右侧先天性膈疝相关，并回顾与先天性膈疝相关的染色体异常的文献

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Chih-Ping Chen; Yeou-Lih Wang; Schu-Rern Chern; Yu-Peng Liu; Cheng-Ran Peng; Yu-Ling Kuo; Peih-Shan Wu; Wen-Lin Chen; Wayseen Wang;
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1. Prenatal diagnosis and array comparative genomic hybridization characterization of trisomy 21 in a fetus associated with right congenital diaphragmatic hernia and a review of the literature of chromosomal abnormalities associated with congenital diaphragmatic hernia [J] . Chen Chih-Ping, Wang Yeou-Lih, Chern Schu-Rern, Taiwanese journal of obstetrics and gynecology . 2015,第1期

机译：胎儿与右先天性diaphragm肌疝相关的21三体综合征的产前诊断和阵列比较基因组杂交表征以及与先天性diaphragm肌疝相关的染色体异常文献综述
2. Prenatal diagnosis and array comparative genomic hybridization characterization of trisomy 21 in a fetus associated with right congenital diaphragmatic hernia and a review of the literature of?chromosomal abnormalities associated with congenital diaphragmatic hernia [J] . Chih-Ping Chen, Yeou-Lih Wang, Schu-Rern Chern, Taiwanese journal of obstetrics and gynecology . 2015,第1期

机译：胎儿与右先天性diaphragm肌疝相关的21三体综合征的产前诊断和阵列比较基因组杂交表征以及与先天性diaphragm肌疝相关的染色体异常文献综述
3. Second-trimester diagnosis of complete trisomy 9 associated with abnormal maternal serum screen results, open sacral spina bifida and congenital diaphragmatic hernia, and review of the literature. [J] . Chen CP, Chern SR, Cheng SJ, Prenatal Diagnosis . 2004,第6期

机译：完全三体9的中期妊娠诊断与异常的产妇血清筛查结果，开放性spin骨脊柱裂和先天性diaphragm肌疝有关，并复习文献。
4. Development of a robotic manipulator system for Congenital Diaphragmatic Hernia [C] . 2011 IEEE International Conference on Systems, Man, and Cybernetics . 2011

机译：先天性Dia肌疝的机械手系统的开发
5. Investigating the mechanisms underlying congenital diaphragmatic hernia and lung maturation. [D] . Branchfield, Kelsey. 2015

机译：研究先天性diaphragm肌疝和肺成熟的潜在机制。
6. Congenital Diaphragmatic Hernia and Chromosome 15q26: Determination of a Candidate Region by Use of Fluorescent In Situ Hybridization and Array-Based Comparative Genomic Hybridization [O] . M. Klaassens, M. van Dooren, H. J. Eussen, 2005

机译：先天性Dia肌疝和染色体15q26：通过使用荧光原位杂交和基于阵列的比较基因组杂交确定候选区域
7. Prenatal diagnosis and array comparative genomic hybridization characterization of trisomy 21 in a fetus associated with right congenital diaphragmatic hernia and a review of the literature of chromosomal abnormalities associated with congenital diaphragmatic hernia [O] . Chen Chih-Ping, Wang Yeou-Lih, Chern Schu-Rern, 2015

机译：右先天性diaphragm肌疝相关胎儿的21三体性的产前诊断和阵列比较基因组杂交表征以及与先天性diaphragm肌疝相关的染色体异常文献综述

Prenatal diagnosis and array comparative genomic hybridization characterization of trisomy 21 in a fetus associated with right congenital diaphragmatic hernia and a review of the literature of chromosomal abnormalities associated with congenital diaphragmatic hernia

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