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Chromosome 13q deletion syndrome involving 13q31-qter: A case report
Partial deletions on the long arm of chromosome 13 lead to a number of different phenotypes depending on the size and position of the deleted region. The present study investigated 2 patients with 13q terminal (13qter) deletion syndrome, which manifested as anal atresia with rectoperineal fistula, c...
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| izdano v: | Mol Med Rep |
|---|---|
| Main Authors: | , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
D.A. Spandidos
2017
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| Teme: | |
| Online dostop: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5436299/ https://ncbi.nlm.nih.gov/pubmed/28393221 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3892/mmr.2017.6425 |
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