Prenatal diagnosis and molecular characterization of a maternally inherited derivative chromosome 9 resulting in a partial deletion 9p(9p22-pter) and partial duplication 18q23.

Escalona Ariadna; Sureda Mnica; Fortuno Joana; Duran Jordi; Caballero Susana; Martin Leonor; Ayensa Fernando; Andreu Sandra

首页> 外文期刊>Chromosome research: An international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology >Prenatal diagnosis and molecular characterization of a maternally inherited derivative chromosome 9 resulting in a partial deletion 9p(9p22-pter) and partial duplication 18q23.

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Prenatal diagnosis and molecular characterization of a maternally inherited derivative chromosome 9 resulting in a partial deletion 9p(9p22-pter) and partial duplication 18q23.

机译：产前遗传衍生物染色体9的产前诊断和分子表征导致部分缺失9p（9p22-pter）和部分复制18q23。

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《Chromosome research: An international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology 》 |2015年第1期| 共2页
作者
Escalona Ariadna; Sureda Mnica; Fortuno Joana; Duran Jordi; Caballero Susana; Martin Leonor; Ayensa Fernando; Andreu Sandra;
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作者单位

Mdb Lab Anal Clin SA Dept Citogenet &

Biol Mol Barcelona Spain;

Mdb Lab Anal Clin SA Dept Citogenet &

Biol Mol Barcelona Spain;

Mdb Lab Anal Clin SA Dept Citogenet &

Biol Mol Barcelona Spain;

Mdb Lab Anal Clin SA Dept Direccio Med Barcelona Spain;

Mdb Lab Anal Clin SA Dept Citogenet &

Biol Mol Barcelona Spain;

Mdb Lab Anal Clin SA Dept Citogenet &

Biol Mol Barcelona Spain;

Mutua Nuestra Senyora Carmen Dept Tocoginecol Granollers Spain;

Mdb Lab Anal Clin SA Dept Citogenet &

Biol Mol Barcelona Spain;

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正文语种 eng
中图分类医学遗传学 ;
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1. Prenatal diagnosis and molecular characterization of a maternally inherited derivative chromosome 9 resulting in a partial deletion 9p(9p22-pter) and partial duplication 18q23. [J] . Escalona Ariadna, Sureda Mnica, Fortuno Joana, Chromosome research: An international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology . 2015 ,第Suppla1期

机译：产前遗传衍生物染色体9的产前诊断和分子表征导致部分缺失9p（9p22-pter）和部分复制18q23。
2. Prenatal molecular cytogenetic analysis of a mild dysmorphic fetus with a huge unbalance karyotype involving partial 9p deletion and partial 18q duplication [J] . Li Yueh-Chun, Pan Yi-Ju, Tsai Fuu-Jen, Genes and genomics . 2016 ,第1期

机译：具有巨大的不平衡核型的轻度畸形胎儿的产前分子细胞遗传学分析，涉及部分9p缺失和部分18q复制
3. 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
4. Combining Duplication, Partial Reconfiguration and Software for On-line Error Diagnosis and Recovery in SRAM-Based FPGAs [C] . Ilias A., Papadimitriou K., Dollas A. 2010 18th IEEE Annual International Symposium on Field-Programmable Custom Computing Machines (FCCM 2010) . 2010

机译：结合了复制，部分重配置和软件，可在基于SRAM的FPGA中进行在线错误诊断和恢复
5. Molecular characterization of citrus partial hybrids produced by microprotoplast mediated chromosome transfer. [D] . Gade, Viola. 2004

机译：微原生质体介导的染色体转移产生的柑橘部分杂种的分子特征。
6. A prenatal diagnosis case of partial duplication 21q21.1-q21.2 with normal phenotype maternally inherited [O] . Chunyan Jin, Zhiping Gu, Xiaohan Jiang, 2021

机译：具有正常表型母系遗传的部分复制21Q21.1-Q21.2的产前诊断案例
7. 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] . Chih-Ping Chen, Chen-Ju Lin, Schu-Rern Chern, 2016

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

Prenatal diagnosis and molecular characterization of a maternally inherited derivative chromosome 9 resulting in a partial deletion 9p(9p22-pter) and partial duplication 18q23.

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