Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Nehama Cohen-Kfir"'
Autor:
Nehama Cohen-Kfir, Miriam Ethel Bentwich, Andrew Kent, Nomy Dickman, Mary Tanus, Basem Higazi, Limor Kalfon, Mary Rudolf, Tzipora C. Falik-Zaccai
Publikováno v:
BMC Medical Ethics, Vol 21, Iss 1, Pp 1-16 (2020)
Abstract Background The Arab population in Israel is a minority ethnic group with its own distinct cultural subgroups. Minority populations are known to underutilize genetic tests and counseling services, thereby undermining the effectiveness of thes
Externí odkaz:
https://doaj.org/article/555e9839e75a4c03a817327808d14cb3
Publikováno v:
Journal of Genetic Counseling. 30:70-74
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::87796282389dc3f72bec3c1785ffcd7b
https://doi.org/10.1002/jgc4.1369
https://doi.org/10.1002/jgc4.1369
Autor:
Tzipora C. Falik-Zaccai, Nurit Edri, Nehama Cohen-Kfir, Irith Weissman, Lena Sagi-Dain, Hadas Shasha Lavski, Limor Kalfon, Amir Peleg
Publikováno v:
Birth Defects Research. 112:316-320
BACKGROUND Isolated populations with high rates of consanguinity and genetic disorders can be found in most parts of the world. The aim of our paper was to highlight the unique challenges faced in genetic counseling for such patients and to discuss t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7ef7b70139a62aaa6e80b6f226baaf45
https://doi.org/10.1002/bdr2.1633
https://doi.org/10.1002/bdr2.1633
Autor:
Miriam Ethel Bentwich, Nomy Dickman, Basem Higazi, Nehama Cohen-Kfir, Mary Rudolf, Tzipora C. Falik-Zaccai, Andrew Kent, Limor Kalfon, Mary Tanus
Publikováno v:
BMC Medical Ethics
BMC Medical Ethics, Vol 21, Iss 1, Pp 1-16 (2020)
BMC Medical Ethics, Vol 21, Iss 1, Pp 1-16 (2020)
BackgroundThe Arab population in Israel is a minority ethnic group with its own distinct cultural subgroups. Minority populations are known to underutilize genetic tests and counseling services, thereby undermining the effectiveness of these services
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c4cbe7ce3d30661b6b574a6ddeae2eb
http://europepmc.org/articles/PMC7565773
http://europepmc.org/articles/PMC7565773
Autor:
Yoav Hoffman, Tzipora C. Falik-Zaccai, Ayelet Eran, Hanna Mandel, Efrat Shuster Biton, Limor Kalfon, April Dinwiddie, Liat Apel‐Sarid, Ayalla Fedida, Elena Dumin, Marwan Odeh, Vered Fleischer Sheffer, Dov Tiosano, Nehama Cohen Kfir, Yael Goldberg, Shani Ben‐Harouch
Publikováno v:
Clinical geneticsREFERENCES. 98(4)
COG6-congenital disorder of glycosylation (COG6-CDG) is caused by biallelic mutations in COG6. To-date, 12 variants causing COG6-CDG in less than 20 patients have been reported. Using whole exome sequencing we identified two siblings with a novel hom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1ee01ef56ca01f23aa4f60a3fe4f4fac
https://pubmed.ncbi.nlm.nih.gov/32683677
https://pubmed.ncbi.nlm.nih.gov/32683677
Autor:
Limor Kalfon, Rotem Paz, Hadas Raveh-Barak, Areef Salama, Nadra Samra, Alexander Kaplun, Natalia Chasnyk, Nehama Cohen Kfir, Nissreen Kinaani Mousa, Efrat Shuster Biton, Mary Tanus, Judith Aharon-Peretz, Tzipora Falik-Zaccai
Publikováno v:
SSRN Electronic Journal.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::255029ba660cf9d110ea0eb4c4d700db
https://doi.org/10.2139/ssrn.3750674
https://doi.org/10.2139/ssrn.3750674