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Z Borochowitz

Showing results (41-50 of 55) with videos related to

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American Journal of Medical Genetics|February 1, 1993
Spondylo-meta-epiphyseal dysplasia (SMED), short limb-hand type: a congenital familial skeletal dysplasia with distinctive features and histopathologyZ Borochowitz, L O Langer, H E Gruber, et al.
The Journal of Clinical Endocrinology and Metabolism|January 1, 1985
Does 1,25-dihydroxyvitamin D participate in the regulation of hormone release from endocrine glands?Z Hochberg, Z Borochowitz, A Benderli, et al.
Prenatal Diagnosis|April 1, 1995
DNA-based carrier detection and prenatal diagnosis of tyrosinase-negative oculocutaneous albinism (OCA1A)T C Falik-Borenstein, S A Holmes, Z Borochowitz, et al.
Fetal Diagnosis and Therapy|March 1, 1995
Very low maternal serum unconjugated estriol and prenatal diagnosis of steroid sulfatase deficiencyM David, N Israel, R Merksamer, et al.
American Journal of Human Genetics|January 1, 1997
Predisposition to the fragile X syndrome in Jews of Tunisian descent is due to the absence of AGG interruptions on a rare Mediterranean haplotypeT C Falik-Zaccai, E Shachak, M Yalon, et al.
Parkinsonism & Related Disorders|August 31, 2015
SMPD1 mutations and Parkinson diseaseE Dagan, V Adir, I Schlesinger, et al.
The Israel Medical Association Journal : IMAJ|September 9, 2000
Achondroplasia in diverse Jewish and Arab populations in Israel: clinical and molecular characterizationT C Falik-Zaccai, E Shachak, D Abeliovitch, et al.
Israel Journal of Medical Sciences|May 1, 1995
Ethnic distribution of the fragile X syndrome in Israel: evidence of founder chromosomes(?)H Dar, T Chemke, T Schaap, et al.
Prenatal Diagnosis|May 23, 2000
DNA based prenatal testing for the skin blistering disorder epidermolysis bullosa simplexE L Rugg, D Baty, C S Shemanko, et al.
European Journal of Human Genetics : EJHG|October 22, 1998
Deletion mapping on chromosome 10p and definition of a critical region for the second DiGeorge syndrome locus (DGS2)S Schuffenhauer, P Lichtner, P Peykar-Derakhshandeh, et al.
Pageof 6

Showing results (41-50 of 55) with videos related to

Sort By:
Pageof 6
American Journal of Medical Genetics|February 1, 1993
Spondylo-meta-epiphyseal dysplasia (SMED), short limb-hand type: a congenital familial skeletal dysplasia with distinctive features and histopathologyZ Borochowitz, L O Langer, H E Gruber, et al.
The Journal of Clinical Endocrinology and Metabolism|January 1, 1985
Does 1,25-dihydroxyvitamin D participate in the regulation of hormone release from endocrine glands?Z Hochberg, Z Borochowitz, A Benderli, et al.
Prenatal Diagnosis|April 1, 1995
DNA-based carrier detection and prenatal diagnosis of tyrosinase-negative oculocutaneous albinism (OCA1A)T C Falik-Borenstein, S A Holmes, Z Borochowitz, et al.
Fetal Diagnosis and Therapy|March 1, 1995
Very low maternal serum unconjugated estriol and prenatal diagnosis of steroid sulfatase deficiencyM David, N Israel, R Merksamer, et al.
American Journal of Human Genetics|January 1, 1997
Predisposition to the fragile X syndrome in Jews of Tunisian descent is due to the absence of AGG interruptions on a rare Mediterranean haplotypeT C Falik-Zaccai, E Shachak, M Yalon, et al.
Parkinsonism & Related Disorders|August 31, 2015
SMPD1 mutations and Parkinson diseaseE Dagan, V Adir, I Schlesinger, et al.
The Israel Medical Association Journal : IMAJ|September 9, 2000
Achondroplasia in diverse Jewish and Arab populations in Israel: clinical and molecular characterizationT C Falik-Zaccai, E Shachak, D Abeliovitch, et al.
Israel Journal of Medical Sciences|May 1, 1995
Ethnic distribution of the fragile X syndrome in Israel: evidence of founder chromosomes(?)H Dar, T Chemke, T Schaap, et al.
Prenatal Diagnosis|May 23, 2000
DNA based prenatal testing for the skin blistering disorder epidermolysis bullosa simplexE L Rugg, D Baty, C S Shemanko, et al.
European Journal of Human Genetics : EJHG|October 22, 1998
Deletion mapping on chromosome 10p and definition of a critical region for the second DiGeorge syndrome locus (DGS2)S Schuffenhauer, P Lichtner, P Peykar-Derakhshandeh, et al.
Pageof 6