Identification of embryonic lethal genes in humans by autozygosity mapping and exome sequencing in consanguineous families

BACKGROUND: Identifying genetic variants that lead to discernible phenotypes is the core of Mendelian genetics. An approach that considers embryonic lethality as a bona fide Mendelian phenotype has the potential to reveal novel genetic causes, which will further our understanding of early human deve...

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Detalles Bibliográficos
Autores principales: Shamseldin, Hanan E., Tulbah, Maha, Kurdi, Wesam, Nemer, Maha, Alsahan, Nada, Al Mardawi, Elham, Khalifa, Ola, Hashem, Amal, Kurdi, Ahmed, Babay, Zainab, Bubshait, Dalal K., Ibrahim, Niema, Abdulwahab, Firdous, Rahbeeni, Zuhair, Hashem, Mais, Alkuraya, Fowzan S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4491988/
https://www.ncbi.nlm.nih.gov/pubmed/26036949
http://dx.doi.org/10.1186/s13059-015-0681-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4491988/
https://www.ncbi.nlm.nih.gov/pubmed/26036949
http://dx.doi.org/10.1186/s13059-015-0681-6

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