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1p36 deletion syndrome: an update
Deletions of chromosome 1p36 affect approximately 1 in 5,000 newborns and are the most common terminal deletions in humans. Medical problems commonly caused by terminal deletions of 1p36 include developmental delay, intellectual disability, seizures, vision problems, hearing loss, short stature, dis...
שמור ב:
| הוצא לאור ב: | Appl Clin Genet |
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| Main Authors: | , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
Dove Medical Press
2015
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4555966/ https://ncbi.nlm.nih.gov/pubmed/26345236 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2147/TACG.S65698 |
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