Recommendation of premarital genetic screening in the Syrian Jewish community based on mutation carrier frequencies within Syrian Jewish cohorts

BACKGROUND: There is a paucity of information available regarding the carrier frequency for autosomal recessive pathogenic variants among Syrian Jews. This report provides data to support carrier screening for a group of autosomal recessive conditions among Syrian Jews based on the population freque...

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Detalles Bibliográficos
Autores principales: Zeevi, David A., Chung, Wendy K., Levi, Chaim, Scher, Sholem Y., Bringer, Rachel, Kahan, Yael, Muallem, Hagit, Benel, Rinat, Hirsch, Yoel, Weiden, Tzvi, Ekstein, Ahron, Ekstein, Josef
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8404236/
https://www.ncbi.nlm.nih.gov/pubmed/34288589
http://dx.doi.org/10.1002/mgg3.1756

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8404236/
https://www.ncbi.nlm.nih.gov/pubmed/34288589
http://dx.doi.org/10.1002/mgg3.1756

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