PubMed ID |
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24143197 |
Publish Date |
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2013 Oct |
Journal |
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PLoS One |
Species |
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Homo sapiens |
Disease Type |
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Cri-du-chat syndrome |
Technology |
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Array CGH |
Case Number |
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2 |
Raw Data |
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Title |
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A Familial Cri-du-Chat/5p Deletion Syndrome Resulted from Rare Maternal Complex Chromosomal Rearrangements (CCRs) and/or Possible Chromosome 5p Chromothripsis |
Authors |
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Heng Gu, Jian-hui Jiang, Jian-ying Li, Ya-nan Zhang, Xing-sheng Dong, Yang-yu Huang, Xinming Son, Xinyan Lu, Zheng Chen |
Affiliation |
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Department of Medical Genetics, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou, PR China |
Chromothripsis Definition |
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Close-by breakpoints: >=6 Copy number states: 2 Fragments random joining: NA |
Download |
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Study Data File |
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Chromothripsis Cases |
mother |
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Case ID: |
mother |
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Chromosome: | 5 |
|
Disease type: |
Cri-du-chat syndrome |
|
Technology: |
Array CGH |
|
Platform: |
Agilent 4x180K array |
|
Affected Gene: |
Gene List |
| | daughter |
|
|
|
|
Case ID: |
daughter |
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Chromosome: | 5 |
|
Disease type: |
Cri-du-chat syndrome |
|
Technology: |
Array CGH |
|
Platform: |
Agilent 4x180K array |
|
Affected Gene: |
Gene List |
| |
|