Targeted genomic capture and massively parallel sequencing to identify genes for hereditary hearing loss in middle eastern families

BACKGROUND: Identification of genes responsible for medically important traits is a major challenge in human genetics. Due to the genetic heterogeneity of hearing loss, targeted DNA capture and massively parallel sequencing are ideal tools to address this challenge. Our subjects for genome analysis...

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Detalles Bibliográficos
Autores principales: Brownstein, Zippora, Friedman, Lilach M, Shahin, Hashem, Oron-Karni, Varda, Kol, Nitzan, Rayyan, Amal Abu, Parzefall, Thomas, Lev, Dorit, Shalev, Stavit, Frydman, Moshe, Davidov, Bella, Shohat, Mordechai, Rahile, Michele, Lieberman, Sari, Levy-Lahad, Ephrat, Lee, Ming K, Shomron, Noam, King, Mary-Claire, Walsh, Tom, Kanaan, Moien, Avraham, Karen B
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3308052/
https://www.ncbi.nlm.nih.gov/pubmed/21917145
http://dx.doi.org/10.1186/gb-2011-12-9-r89

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3308052/
https://www.ncbi.nlm.nih.gov/pubmed/21917145
http://dx.doi.org/10.1186/gb-2011-12-9-r89

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