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Moshe Frydman

Showing results (1-10 of 43) with videos related to

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The Israel Medical Association Journal : IMAJ|May 23, 2008
The Marfan syndromeMoshe Frydman
Journal of Children'S Orthopaedics|April 2, 2011
Historical note: an analysis of a 17th century illustration of a child with split hand/split foot malformationAvi Ohry, Moshe Frydman
Journal of Basic and Clinical Physiology and Pharmacology|August 26, 2014
Apparent phenotypic anticipation in autosomal dominant connexin 26 deafnessMeirav Sokolov, Zippora Brownstein, Moshe Frydman, et al.
Journal of Child Language|March 29, 2006
Language in boys with fragile X syndromeYonata Levy, Riki Gottesman, Zvi Borochowitz, et al.
European Journal of Dermatology : EJD|September 21, 2005
Confirmation of the association between male pattern baldness and the androgen receptor geneEtgar Levy-Nissenbaum, Michal Bar-Natan, Moshe Frydman, et al.
Archives of Otolaryngology--Head & Neck Surgery|April 19, 2006
Chromosomal mapping and phenotypic characterization of hereditary otosclerosis linked to the OTSC4 locusZippora Brownstein, Abraham Goldfarb, Haya Levi, et al.
Experimental Dermatology|June 30, 2015
Autosomal-dominant cutis laxa resulting from an intronic mutation in ELNDan Vodo, Ofer Sarig, Alon Peled, et al.
Journal of Medical Screening|December 14, 2011
The D1152H cystic fibrosis mutation in prenatal carrier screening, patients and prenatal diagnosisLeah Peleg, Mazal Karpati, Silvia Bronstein, et al.
World Journal of Gastroenterology|December 18, 2014
Late onset fulminant Wilson's disease: a case report and review of the literatureElla Weitzman, Orit Pappo, Peretz Weiss, et al.
American Journal of Human Genetics|May 3, 2008
Deleterious mutations in the Zinc-Finger 469 gene cause brittle cornea syndromeAlmogit Abu, Moshe Frydman, Dina Marek, et al.
Pageof 5

Showing results (1-10 of 43) with videos related to

Sort By:
Pageof 5
The Israel Medical Association Journal : IMAJ|May 23, 2008
The Marfan syndromeMoshe Frydman
Journal of Children'S Orthopaedics|April 2, 2011
Historical note: an analysis of a 17th century illustration of a child with split hand/split foot malformationAvi Ohry, Moshe Frydman
Journal of Basic and Clinical Physiology and Pharmacology|August 26, 2014
Apparent phenotypic anticipation in autosomal dominant connexin 26 deafnessMeirav Sokolov, Zippora Brownstein, Moshe Frydman, et al.
Journal of Child Language|March 29, 2006
Language in boys with fragile X syndromeYonata Levy, Riki Gottesman, Zvi Borochowitz, et al.
European Journal of Dermatology : EJD|September 21, 2005
Confirmation of the association between male pattern baldness and the androgen receptor geneEtgar Levy-Nissenbaum, Michal Bar-Natan, Moshe Frydman, et al.
Archives of Otolaryngology--Head & Neck Surgery|April 19, 2006
Chromosomal mapping and phenotypic characterization of hereditary otosclerosis linked to the OTSC4 locusZippora Brownstein, Abraham Goldfarb, Haya Levi, et al.
Experimental Dermatology|June 30, 2015
Autosomal-dominant cutis laxa resulting from an intronic mutation in ELNDan Vodo, Ofer Sarig, Alon Peled, et al.
Journal of Medical Screening|December 14, 2011
The D1152H cystic fibrosis mutation in prenatal carrier screening, patients and prenatal diagnosisLeah Peleg, Mazal Karpati, Silvia Bronstein, et al.
World Journal of Gastroenterology|December 18, 2014
Late onset fulminant Wilson's disease: a case report and review of the literatureElla Weitzman, Orit Pappo, Peretz Weiss, et al.
American Journal of Human Genetics|May 3, 2008
Deleterious mutations in the Zinc-Finger 469 gene cause brittle cornea syndromeAlmogit Abu, Moshe Frydman, Dina Marek, et al.
Pageof 5