Identification of Novel Risk Variants of Non-Syndromic Cleft Palate by Targeted Gene Panel Sequencing

Non-syndromic cleft palate (ns-CP) has a genetically heterogeneous aetiology. Numerous studies have suggested a crucial role of rare coding variants in characterizing the unrevealed component of genetic variation in ns-CP called the “missing heritability”. Therefore, this study aimed to detect low-f...

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Detalles Bibliográficos
Autores principales: Dąbrowska, Justyna, Biedziak, Barbara, Bogdanowicz, Agnieszka, Mostowska, Adrianna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10004578/
https://www.ncbi.nlm.nih.gov/pubmed/36902838
http://dx.doi.org/10.3390/jcm12052051

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10004578/
https://www.ncbi.nlm.nih.gov/pubmed/36902838
http://dx.doi.org/10.3390/jcm12052051

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