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Prenatal diagnosis and molecular cytogenetic characterization of a de novo unbalanced reciprocal translocation of der(9)t(9;14)(p24.2;q32.11) associated with 9p terminal deletion and 14q distal duplication

机译：产前诊断和分子细胞遗传学表征der（9）t（9; 14）（p24.2; q32.11）与9p末端缺失和14q远端重复相关的从头不平衡相互易位

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Chih-Ping Chen; Chen-Ju Lin; Schu-Rern Chern; Peih-Shan Wu; Yen-Ni Chen; Shin-Wen Chen; Chen-Chi Lee; Li-Feng Chen; Chien-Wen Yang; Wayseen Wang;
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1. Prenatal diagnosis and molecular cytogenetic characterization of a de novo unbalanced reciprocal translocation of der(9) t(9;14)(p24.2;q32.11) associated with 9p terminal deletion and 14q distal duplication [J] . Chen Chih-Ping, Lin Chen-Ju, Chern Schu-Rern, Taiwanese journal of obstetrics and gynecology . 2016,第4期

机译：与9p末端缺失和14q远端复制相关的der（9）t（9; 14）（p24.2; q32.11）从头不平衡反向转运的产前诊断和分子细胞遗传学特征
2. Prenatal diagnosis and molecular cytogenetic characterization of a de novo unbalanced reciprocal translocation of der(9)t(9;14)(p24.2;q32.11) associated with 9p terminal deletion and 14q distal duplication [J] . Chih-Ping Chen, Chen-Ju Lin, Schu-Rern Chern, Taiwanese journal of obstetrics and gynecology . 2016,第4期

机译：与9p末端缺失和相关的der（9）t（9; 14）（p24.2; q32.11）互不平衡的 de novo 不平衡倒易位的产前诊断和分子细胞遗传学特征14q远端复制
3. De novo unbalanced translocation resulting in monosomy for distal 5p (5p14.1? →?pter) and 14q (14q32.31? →?qter) associated with fetal nuchal edema, microcephaly, intrauterine growth restriction, and single umbilical artery: Prenatal diagnosis and molecular cytogenetic characterization [J] . Chih-Ping Chen, Chung-Hu Fu, Schu-Rern Chern, Taiwanese journal of obstetrics and gynecology . 2013,第3期

机译：从头的不平衡移位导致远端5p（5p14.1？→？pter）和14q（14q32.31？→？qter）与胎儿颈部水肿，小头畸形，宫内生长受限和单条脐动脉相关：产前诊断和分子细胞遗传学特征
4. A rare de novo duplication of chromosome 21q22.12 → q22.3 with other concomitant deletion and duplication of small fragments in 21q associated with Down syndrome: Prenatal diagnosis molecular cytogenetic characterization [O] . Qingwei Qi, Xiya Zhou, Yulin Jiang, 2013

机译：罕见的从头复制21q22.12→q22.3染色体以及与唐氏综合症相关的21q小片段的其他伴随缺失和重复：产前诊断分子细胞遗传学表征
5. Prenatal diagnosis and molecular cytogenetic characterization of a de novo unbalanced reciprocal translocation of der(9)t(9;14)(p24.2;q32.11) associated with 9p terminal deletion and 14q distal duplication [O] . Chen Chih-Ping, Lin Chen-Ju, Chern Schu-Rern, 2016

机译：与9p末端缺失和14q远端复制相关的der（9）t（9; 14）（p24.2; q32.11）从头不平衡反向转运的产前诊断和分子细胞遗传学特征

Prenatal diagnosis and molecular cytogenetic characterization of a de novo unbalanced reciprocal translocation of der(9)t(9;14)(p24.2;q32.11) associated with 9p terminal deletion and 14q distal duplication

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