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Copy Number Changes Identified Using Whole Exome Sequencing in Non-Syndromic Cleft Lip and Palate in a Honduran Population
BACKGROUND: The majority of cleft lip with or without cleft palate (CL/P) cases appear as an isolated, non-syndromic entity (NSCLP). With the advent of next generation sequencing, whole exome sequencing (WES) has been used to identify single nucleotide variants and insertion/deletions which cause or...
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| Publicat a: | Birth Defects Res |
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| Autors principals: | , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2017
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5854563/ https://ncbi.nlm.nih.gov/pubmed/28748635 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/bdr2.1063 |
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