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M Frydman

Showing results (151-160 of 172) with videos related to

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Human Genetics|November 1, 1988
Linkage studies do not confirm the cytogenetic location of incontinentia pigmenti on Xp11A Sefiani, D Sinnett, L Abel, et al.
Annals of Human Genetics|May 1, 1990
Wilson's disease in Israel: a genetic and epidemiological studyB Bonné-Tamir, M Frydman, M S Agger, et al.
American Journal of Medical Genetics|July 1, 1990
Possible heterogeneity in spondyloenchondrodysplasia: quadriparesis, basal ganglia calcifications, and chondrocyte inclusionsM Frydman, J Bar-Ziv, R Preminger-Shapiro, et al.
The Israel Medical Association Journal : IMAJ|August 25, 2001
A gene causing autosomal recessive cataract maps to the short arm of chromosome 3E Pras, E Pras, T Bakhan, et al.
Human Genetics|September 12, 2000
The prevalence and expression of inherited connexin 26 mutations associated with nonsyndromic hearing loss in the Israeli populationT Sobe, S Vreugde, H Shahin, et al.
American Journal of Human Genetics|June 1, 1996
Linkage of congenital recessive deafness (gene DFNB10) to chromosome 21q22.3B Bonné-Tamir, A L DeStefano, C E Briggs, et al.
Neurology|July 1, 1991
Predictive testing for Wilson's disease using tightly linked and flanking DNA markersL A Farrer, A M Bowcock, J M Hebert, et al.
American Journal of Human Genetics|November 1, 1988
Eight closely linked loci place the Wilson disease locus within 13q14-q21A M Bowcock, L A Farrer, J M Hebert, et al.
Human Mutation|February 5, 1998
Identification of ATM mutations using extended RT-PCR and restriction endonuclease fingerprinting, and elucidation of the repertoire of A-T mutations in IsraelS Gilad, R Khosravi, R Harnik, et al.
Journal of Molecular Biology|October 20, 1993
Molecular characterization of the DNA puff C-8 gene of Rhynchosciara americanaH M Frydman, E O Cadavid, J Yokosawa, et al.
Pageof 18

Showing results (151-160 of 172) with videos related to

Sort By:
Pageof 18
Human Genetics|November 1, 1988
Linkage studies do not confirm the cytogenetic location of incontinentia pigmenti on Xp11A Sefiani, D Sinnett, L Abel, et al.
Annals of Human Genetics|May 1, 1990
Wilson's disease in Israel: a genetic and epidemiological studyB Bonné-Tamir, M Frydman, M S Agger, et al.
American Journal of Medical Genetics|July 1, 1990
Possible heterogeneity in spondyloenchondrodysplasia: quadriparesis, basal ganglia calcifications, and chondrocyte inclusionsM Frydman, J Bar-Ziv, R Preminger-Shapiro, et al.
The Israel Medical Association Journal : IMAJ|August 25, 2001
A gene causing autosomal recessive cataract maps to the short arm of chromosome 3E Pras, E Pras, T Bakhan, et al.
Human Genetics|September 12, 2000
The prevalence and expression of inherited connexin 26 mutations associated with nonsyndromic hearing loss in the Israeli populationT Sobe, S Vreugde, H Shahin, et al.
American Journal of Human Genetics|June 1, 1996
Linkage of congenital recessive deafness (gene DFNB10) to chromosome 21q22.3B Bonné-Tamir, A L DeStefano, C E Briggs, et al.
Neurology|July 1, 1991
Predictive testing for Wilson's disease using tightly linked and flanking DNA markersL A Farrer, A M Bowcock, J M Hebert, et al.
American Journal of Human Genetics|November 1, 1988
Eight closely linked loci place the Wilson disease locus within 13q14-q21A M Bowcock, L A Farrer, J M Hebert, et al.
Human Mutation|February 5, 1998
Identification of ATM mutations using extended RT-PCR and restriction endonuclease fingerprinting, and elucidation of the repertoire of A-T mutations in IsraelS Gilad, R Khosravi, R Harnik, et al.
Journal of Molecular Biology|October 20, 1993
Molecular characterization of the DNA puff C-8 gene of Rhynchosciara americanaH M Frydman, E O Cadavid, J Yokosawa, et al.
Pageof 18