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Page 1
Patients' Attitudes Towards Disclosure of Genetic Test Results to Family Members: The Impact of Patients' Sociodemographic Background and Counseling Experience.
Gilbar R, Shalev S, Spiegel R, Pras E, Berkenstadt M, Sagi M, Ben-Yehuda A, Mor P, Perry S, Zaccai TF, Borochowitz Z, Barnoy S. Gilbar R, et al. Among authors: borochowitz z. J Genet Couns. 2016 Apr;25(2):314-24. doi: 10.1007/s10897-015-9873-1. Epub 2015 Sep 14. J Genet Couns. 2016. PMID: 26371363
[60 years of medical genetics in Israel].
Shalev SA, Borochowitz ZU, Zlotogora J. Shalev SA, et al. Harefuah. 2010 Feb;149(2):91-4, 124. Harefuah. 2010. PMID: 20549926 Review. Hebrew.
Response to 'Darier disease in Israel: combined evaluation of genetic and neuropsychiatric aspects': reply from the authors.
Dodiuk-Gad RP, Cohen-Barak E, Khayat M, Milo H, Amariglio-Diskin L, Danial-Faran N, Sah M, Ziv M, Shani-Adir A, Amichai B, Zlotogorski A, Borochowitz Z, Rozenman D, Shalev S. Dodiuk-Gad RP, et al. Among authors: borochowitz z. Br J Dermatol. 2016 Jul;175(1):224. doi: 10.1111/bjd.14544. Epub 2016 Jun 7. Br J Dermatol. 2016. PMID: 27272550 No abstract available.
Darier disease in Israel: combined evaluation of genetic and neuropsychiatric aspects.
Dodiuk-Gad RP, Cohen-Barak E, Khayat M, Milo H, Amariglio-Diskin L, Danial-Faran N, Sah M, Ziv M, Shani-Adir A, Amichai B, Zlotogorski A, Borochowitz Z, Rozenman D, Shalev S. Dodiuk-Gad RP, et al. Among authors: borochowitz z. Br J Dermatol. 2016 Mar;174(3):562-8. doi: 10.1111/bjd.14220. Epub 2015 Dec 17. Br J Dermatol. 2016. PMID: 26471493
Language in boys with fragile X syndrome.
Levy Y, Gottesman R, Borochowitz Z, Frydman M, Sagi M. Levy Y, et al. Among authors: borochowitz z. J Child Lang. 2006 Feb;33(1):125-44. doi: 10.1017/s030500090500718x. J Child Lang. 2006. PMID: 16566323
Founder mutation for Huntington disease in Caucasus Jews.
Melamed O, Behar DM, Bram C, Magal N, Pras E, Reznik-Wolf H, Borochowitz ZU, Davidov B, Mor-Cohen R, Baris HN. Melamed O, et al. Among authors: borochowitz zu. Clin Genet. 2015 Feb;87(2):167-72. doi: 10.1111/cge.12344. Epub 2014 Feb 4. Clin Genet. 2015. PMID: 24405192
90 results