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Chromosome 1p32-p31 deletion syndrome: Prenatal diagnosis by array comparative genomic hybridization using uncultured amniocytes and association with NFIA haploinsufficiency, ventriculomegaly, corpus callosum hypogenesis, abnormal external genitalia, and intrauterine growth restriction

机译：染色体1p32-p31缺失综合征：使用未培养的羊水细胞进行阵列比较基因组杂交的产前诊断以及与NFIa单倍体不足，脑室扩大，胼call体低发生，异常外生殖器和胎儿宫内生长受限的关联

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Chih-Ping Chen; Yi-Ning Su; Yi-Yung Chen; Schu-Rern Chern; Yu-Peng Liu; Pei-Chen Wu; Chen-Chi Lee; Yu-Ting Chen; Wayseen Wang;
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年度 2011
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1. Chromosome 1p32-p31 deletion syndrome: Prenatal diagnosis by array comparative genomic hybridization using uncultured amniocytes and association with NFIA haploinsufficiency, ventriculomegaly, corpus callosum hypogenesis, abnormal external genitalia, and intrauterine growth restriction [J] . Taiwanese journal of obstetrics and gynecology . 2011,第3期

机译：1p32-p31染色体缺失综合征：使用未培养的羊细胞通过阵列比较基因组杂交并与NFIA单倍功能不全，心室肥大，call体发育不全，异常的外生殖器和子宫内生长受限相关的阵列比较基因组杂交进行产前诊断
2. Chromosome 1p32-p31 deletion syndrome: Prenatal diagnosis by array comparative genomic hybridization using uncultured amniocytes and association with NFIA haploinsufficiency, ventriculomegaly, corpus callosum hypogenesis, abnormal external genitalia, and intrauterine growth?restriction [J] . Chih-Ping Chen, Yi-Ning Su, Yi-Yung Chen, Taiwanese journal of obstetrics and gynecology . 2011,第3期

机译：1p32-p31染色体缺失综合征：使用未培养的羊细胞通过阵列比较基因组杂交并与 NFIA 单倍体功能不全，心室肥大，体发育不全，异常外生殖器和子宫内生长受限相关的产前诊断
3. Prenatal diagnosis of chromosome 8p23.1 microdeletion by array comparative genomic hybridization using uncultured amniocytes in a pregnancy associated with fetal partial corpus callosum agenesis and schizencephaly [J] . Chen Chih-Ping, Peng Cheng-Ran, Chang Tung-Yao, Taiwanese journal of obstetrics and gynecology . 2015,第6期

机译：在未怀孕的胎儿部分体发育不全和裂脑相关的妊娠中，使用未培养的羊细胞进行阵列比较基因组杂交，对染色体8p23.1微缺失进行产前诊断。
4. Prenatal diagnosis of genomic disorders and chromosome abnormalities using array-based comparative genomic hybridization [O] . Francesca Gullotta, Michela Biancolella, Elena Costa, 2007

机译：使用基于阵列的比较基因组杂交对基因组疾病和染色体异常进行产前诊断
5. Chromosome 1p32-p31 deletion syndrome: Prenatal diagnosis by array comparative genomic hybridization using uncultured amniocytes and association with NFIA haploinsufficiency, ventriculomegaly, corpus callosum hypogenesis, abnormal external genitalia, and intrauterine growth restriction [O] . Chen Chih-Ping, Su Yi-Ning, Chen Yi-Yung, 2011

机译：1p32-p31染色体缺失综合征：使用未培养的羊细胞通过阵列比较基因组杂交并与NFIA单倍功能不全，心室肥大，call体发育不全，外生殖器异常和子宫内生长受限相关的阵列比较基因组杂交进行产前诊断

Chromosome 1p32-p31 deletion syndrome: Prenatal diagnosis by array comparative genomic hybridization using uncultured amniocytes and association with NFIA haploinsufficiency, ventriculomegaly, corpus callosum hypogenesis, abnormal external genitalia, and intrauterine growth restriction

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