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Mosaic deletion-duplication syndrome of chromosome 3: Prenatal molecular cytogenetic diagnosis using cultured and uncultured amniocytes and association with fetoplacental discrepancy

机译：染色体3的马赛克缺失 - 重复综合征：使用培养和未培养的羊水细胞进行产前分子细胞遗传学诊断并与胎儿胎盘差异相关联

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Chih-Ping Chen; Yi-Ning Su; Chin-Yuan Hsu; Schu-Rern Chern; Chen-Chi Lee; Yu-Ting Chen; Wen-Lin Chen; Wayseen Wang;
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年度 2011
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1. Mosaic deletion-duplication syndrome of chromosome 3: Prenatal molecular cytogenetic diagnosis using cultured and uncultured amniocytes and association with fetoplacental discrepancy [J] . ChenC.-P., SuY.-N., HsuC.-Y., Taiwanese journal of obstetrics and gynecology . 2011,第4期

机译：染色体3的马赛克缺失-复制综合征：使用培养和未培养的羊血细胞的胎儿产前细胞遗传学诊断以及与胎盘差异
2. Mosaic deletion-duplication syndrome of chromosome 3: Prenatal molecular cytogenetic diagnosis using cultured and uncultured amniocytes and association with fetoplacental discrepancy [J] . Chih-Ping Chen, Yi-Ning Su, Chin-Yuan Hsu, Taiwanese journal of obstetrics and gynecology . 2011,第4期

机译：染色体3的马赛克缺失-复制综合征：使用培养和未培养的羊细胞进行产前分子细胞遗传学诊断，并与胎儿胎盘差异相关
3. Prenatal diagnosis of low-level mosaicism for a small supernumerary marker chromosome derived from chromosome 9q (9q13-q21.33) in a pregnancy with a favorable outcome, and cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes [J] . Chih-Ping Chen, Liang-Ming Lo, Tsang-Ming Ko, Taiwanese journal of obstetrics and gynecology . 2021,第2期

机译：染色体9Q（9Q13-Q21.33）中源自染色体9Q（9Q13-Q21.33）的低水平马赛瑟的产前诊断具有良好的结果，培养的肿瘤和未培养的羊膜细胞之间的细胞遗传学差异
4. Prenatal Diagnosis of CLOVES Syndrome Confirmed by Detection of a Mosaic PIK3CA Mutation in Cultured Amniocytes [O] . Lisa T. Emrick, Lauren Murphy, Alireza A. Shamshirsaz, -1

机译：通过检测培养的羊膜细胞中的镶嵌PIK3CA突变证实了克洛夫综合征的产前诊断。
5. Mosaic deletion-duplication syndrome of chromosome 3: Prenatal molecular cytogenetic diagnosis using cultured and uncultured amniocytes and association with fetoplacental discrepancy [O] . Chen Chih-Ping, Su Yi-Ning, Hsu Chin-Yuan, 2011

机译：染色体3的镶嵌缺失-复制综合征：使用培养和未培养的羊血细胞的胎儿产前细胞遗传学诊断以及与胎盘差异

Mosaic deletion-duplication syndrome of chromosome 3: Prenatal molecular cytogenetic diagnosis using cultured and uncultured amniocytes and association with fetoplacental discrepancy

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