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20p12.3 deletion is rare cause of syndromic cleft palate: case report and review of literature
BACKGROUND: Orofacial cleft (OFC) is one of the most common congenital malformations with a global incidence of approximately 1/700 live births. Clinically, OFCs can be syndromic or non-syndromic. CASE PRESENTATION: A 5 years old boy admitted for genetic evaluation because of psychomotor delay, fail...
Tallennettuna:
| Julkaisussa: | BMC Res Notes |
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| Päätekijät: | , , , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
BioMed Central
2016
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4698322/ https://ncbi.nlm.nih.gov/pubmed/26724919 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13104-015-1828-y |
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