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

被引：0
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作者：
Qingwei Qi
Xiya Zhou
Yulin Jiang
Na Hao
Jing Zhou
Liang Zhang
机构：
[1] Peking Union Medical College,Department of Obstetrics & Gynecology, Peking Union Medical College Hospital, Chinese Academy of Medical Science
[2] Dongdan,undefined
[3] BioChain (Beijing) Science & Technology Inc.,undefined
来源：
Molecular Cytogenetics | / 6卷
关键词：
Array comparative genomic hybridization (aCGH); Fluorescence in situ hybridization (FISH); Sequence-tagged site (STS); Partial duplication; Prenatal diagnosis; Down syndrome;
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