Prenatal diagnosis of a fetus with ring chromosome 15 characterized by array-CGH

被引:5
|
作者
Manolakos, Emmanouil [1 ]
Vetro, Annalisa [2 ]
Kitmirides, Stylianos [3 ]
Papoulidis, Ioannis [4 ]
Kosyakova, Nadezda [5 ]
Mrasek, Kristin [5 ]
Weise, Anja [5 ]
Agapitos, Emmanouil [6 ]
Orru, Sandro [7 ]
Peitsidis, Panagiotis [8 ]
Liehr, Thomas [5 ]
Petersen, Michael B. [9 ]
机构
[1] Bioiatriki SA, Lab Mol Cytogenet, GR-11526 Athens, Greece
[2] Univ Pavia, Sez Biol Gen & Genet Med, Dipartimento Patol Uman & Ereditaria, I-27100 Pavia, Italy
[3] Fetal Maternal Med Ctr, Athens, Greece
[4] Eurogenetica SA, Lab Mol Biol Genet & Biotechnol, Thessaloniki, Greece
[5] Univ Klinikum Jena, Inst Humangenet & Anthropol, Jena, Germany
[6] Univ Athens, Sch Med, Dept Pathol, GR-10679 Athens, Greece
[7] Univ Cagliari, Dept Med Genet, I-09124 Cagliari, Italy
[8] Royal Free Hosp, Dept Fetal Med, London NW3 2QG, England
[9] Inst Child Hlth, Dept Genet, Athens, Greece
关键词
ring chromosome 15; prenatal diagnosis; array-CGH; deletion; 15q; congenital diaphragmatic hernia; CONGENITAL DIAPHRAGMATIC-HERNIA; GROWTH-RETARDATION; REGION; 15Q26;
D O I
10.1002/pd.2295
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
[No abstract available]
引用
收藏
页码:884 / 888
页数:5
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