Zvi U. Borochowitz
Haifa, HA, Israel
Last Updated: 09/26/2026
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Found 13 publications
Gain-of-function mutation of microRNA-140 in human skeletal dysplasia.
Journal: Nature medicine
Published: December 04, 2017
Response to 'Darier disease in Israel: combined evaluation of genetic and neuropsychiatric aspects': reply from the authors.
Journal: The British journal of dermatology
Published: June 09, 2016
Darier disease in Israel: combined evaluation of genetic and neuropsychiatric aspects.
Journal: The British journal of dermatology
Published: October 05, 2015
SMPD1 mutations and Parkinson disease.
Journal: Parkinsonism & related disorders
Published: August 10, 2015
Patients' Attitudes Towards Disclosure of Genetic Test Results to Family Members: The Impact of Patients' Sociodemographic Background and Counseling Experience.
Journal: Journal of genetic counseling
Published: May 20, 2014
Founder mutation for Huntington disease in Caucasus Jews.
Journal: Clinical genetics
Published: October 01, 2013
BRCA1/2 mutations and FMR1 alleles are randomly distributed: a case control study.
Journal: European journal of human genetics : EJHG
Published: August 21, 2013
Morbid obesity resulting from inactivation of the ciliary protein CEP19 in humans and mice.
Journal: American journal of human genetics
Published: June 21, 2013
Novel SMARCAL1 bi-allelic mutations associated with a chromosomal breakage phenotype in a severe SIOD patient.
Journal: Journal of clinical immunology
Published: June 20, 2013
Early metabolic defects in Arab subjects with strong family history of Type 2 diabetes.
Journal: Journal of endocrinological investigation
Published: December 06, 2012
A system for exact and approximate genetic linkage analysis of SNP data in large pedigrees.
Journal: Bioinformatics (Oxford, England)
Published: November 20, 2012
Last Updated: 09/26/2026