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Zvi U Borochowitz

Showing results (1-10 of 14) with videos related to

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Paediatrics & Child Health|May 14, 2009
Case 2: Developmental delay, especially language, in a toddlerMoshe Shapira, Zvi U Borochowitz
Community Genetics|June 1, 2005
Attitudes of Israeli Muslims at risk of genetic disorders towards pregnancy terminationEfrat Neter, Yael Wolowelsky, Zvi U Borochowitz
European Journal of Medical Genetics|March 24, 2012
A distinctive autosomal recessive syndrome of severe disproportionate short stature with short long bones, brachydactyly, and hypotrichosis in two consanguineous Arab familiesStavit A Shalev, Ronen Spiegel, Zvi U Borochowitz
Harefuah|June 17, 2010
[60 years of medical genetics in Israel]Stavit A Shalev, Zvi U Borochowitz, Joel Zlotogora
Genetic Testing|March 6, 2004
Detection of X chromosome aneuploidy using Southern blot analysis during routine population-based screening for fragile X syndromeVardit Adir, Elena Shahak, Hanna Dar, et al.
Muscle & Nerve|August 22, 2009
Myotonia congenita in a large consanguineous Arab family: insight into the clinical spectrum of carriers and double heterozygotes of a novel mutation in the chloride channel CLCN1 geneAdel Shalata, Haya Furman, Vardit Adir, et al.
Journal of Clinical Immunology|November 8, 2013
Novel SMARCAL1 bi-allelic mutations associated with a chromosomal breakage phenotype in a severe SIOD patientAmos J Simon, Atar Lev, Marta Jeison, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 7, 2009
Dynamic modification strategy of the Israeli prenatal carrier screening protocol: inclusion of the oriental Jewish group to the cystic fibrosis panel-updateOrit Reish, Mordechai Shohat, Nurit Magal, et al.
American Journal of Human Genetics|January 9, 2008
SERKAL syndrome: an autosomal-recessive disorder caused by a loss-of-function mutation in WNT4Hannah Mandel, Revital Shemer, Zvi U Borochowitz, et al.
Bioinformatics (Oxford, England)|November 20, 2012
A system for exact and approximate genetic linkage analysis of SNP data in large pedigreesMark Silberstein, Omer Weissbrod, Lars Otten, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
Paediatrics & Child Health|May 14, 2009
Case 2: Developmental delay, especially language, in a toddlerMoshe Shapira, Zvi U Borochowitz
Community Genetics|June 1, 2005
Attitudes of Israeli Muslims at risk of genetic disorders towards pregnancy terminationEfrat Neter, Yael Wolowelsky, Zvi U Borochowitz
European Journal of Medical Genetics|March 24, 2012
A distinctive autosomal recessive syndrome of severe disproportionate short stature with short long bones, brachydactyly, and hypotrichosis in two consanguineous Arab familiesStavit A Shalev, Ronen Spiegel, Zvi U Borochowitz
Harefuah|June 17, 2010
[60 years of medical genetics in Israel]Stavit A Shalev, Zvi U Borochowitz, Joel Zlotogora
Genetic Testing|March 6, 2004
Detection of X chromosome aneuploidy using Southern blot analysis during routine population-based screening for fragile X syndromeVardit Adir, Elena Shahak, Hanna Dar, et al.
Muscle & Nerve|August 22, 2009
Myotonia congenita in a large consanguineous Arab family: insight into the clinical spectrum of carriers and double heterozygotes of a novel mutation in the chloride channel CLCN1 geneAdel Shalata, Haya Furman, Vardit Adir, et al.
Journal of Clinical Immunology|November 8, 2013
Novel SMARCAL1 bi-allelic mutations associated with a chromosomal breakage phenotype in a severe SIOD patientAmos J Simon, Atar Lev, Marta Jeison, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 7, 2009
Dynamic modification strategy of the Israeli prenatal carrier screening protocol: inclusion of the oriental Jewish group to the cystic fibrosis panel-updateOrit Reish, Mordechai Shohat, Nurit Magal, et al.
American Journal of Human Genetics|January 9, 2008
SERKAL syndrome: an autosomal-recessive disorder caused by a loss-of-function mutation in WNT4Hannah Mandel, Revital Shemer, Zvi U Borochowitz, et al.
Bioinformatics (Oxford, England)|November 20, 2012
A system for exact and approximate genetic linkage analysis of SNP data in large pedigreesMark Silberstein, Omer Weissbrod, Lars Otten, et al.
Pageof 2