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Moshe Frydman

Showing results (11-20 of 43) with videos related to

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American Journal of Medical Genetics. Part A|November 1, 2008
Multiple congenital skull fractures as a presentation of Ehlers-Danlos syndrome type VIICOmer Bar-Yosef, Sylvie Polak-Charcon, Chen Hoffman, et al.
American Journal of Medical Genetics|September 5, 2002
Genetic counseling in hereditary breast/ovarian cancer in Israel: psychosocial impact and retention of genetic informationMichal DiCastro, Moshe Frydman, Irit Friedman, et al.
Journal of Clinical Immunology|January 26, 2010
Leukocyte adhesion deficiency type II: long-term follow-up and review of the literatureYael Gazit, Adi Mory, Amos Etzioni, et al.
Molecular Vision|April 4, 2008
Autosomal dominant congenital cataract in a Libyan Jewish family: cosegregation with a reciprocal chromosomal translocation [t(3;5)(p22.3; p15.1)]Emre Zafer, Jeanne Meck, Liora Gerrad, et al.
Investigative Ophthalmology & Visual Science|May 27, 2004
A nonsense mutation in the glucosaminyl (N-acetyl) transferase 2 gene (GCNT2): association with autosomal recessive congenital cataractsEran Pras, Judith Raz, Vered Yahalom, et al.
Investigative Ophthalmology & Visual Science|November 24, 2006
Mapping of a gene causing brittle cornea syndrome in Tunisian jews to 16q24Almogit Abu, Moshe Frydman, Dina Marek, et al.
Journal of Applied Genetics|May 18, 2011
X inactivation testing for identifying a non-syndromic X-linked mental retardation geneHagith Yonath, Dina Marek-Yagel, Haike Resnik-Wolf, et al.
Human Mutation|March 17, 2004
Genetic and biochemical analyses of Israeli osteogenesis imperfecta patientsLiat Ries-Levavi, Tsofia Ish-Shalom, Moshe Frydman, et al.
American Journal of Human Genetics|March 28, 2002
A missense mutation in the LIM2 gene is associated with autosomal recessive presenile cataract in an inbred Iraqi Jewish familyEran Pras, Etgar Levy-Nissenbaum, Tangiz Bakhan, et al.
Archives of Otolaryngology--Head & Neck Surgery|May 17, 2006
Connexin-associated deafness and speech perception outcome of cochlear implantationRiki Taitelbaum-Swead, Zippora Brownstein, Chava Muchnik, et al.
Pageof 5

Showing results (11-20 of 43) with videos related to

Sort By:
Pageof 5
American Journal of Medical Genetics. Part A|November 1, 2008
Multiple congenital skull fractures as a presentation of Ehlers-Danlos syndrome type VIICOmer Bar-Yosef, Sylvie Polak-Charcon, Chen Hoffman, et al.
American Journal of Medical Genetics|September 5, 2002
Genetic counseling in hereditary breast/ovarian cancer in Israel: psychosocial impact and retention of genetic informationMichal DiCastro, Moshe Frydman, Irit Friedman, et al.
Journal of Clinical Immunology|January 26, 2010
Leukocyte adhesion deficiency type II: long-term follow-up and review of the literatureYael Gazit, Adi Mory, Amos Etzioni, et al.
Molecular Vision|April 4, 2008
Autosomal dominant congenital cataract in a Libyan Jewish family: cosegregation with a reciprocal chromosomal translocation [t(3;5)(p22.3; p15.1)]Emre Zafer, Jeanne Meck, Liora Gerrad, et al.
Investigative Ophthalmology & Visual Science|May 27, 2004
A nonsense mutation in the glucosaminyl (N-acetyl) transferase 2 gene (GCNT2): association with autosomal recessive congenital cataractsEran Pras, Judith Raz, Vered Yahalom, et al.
Investigative Ophthalmology & Visual Science|November 24, 2006
Mapping of a gene causing brittle cornea syndrome in Tunisian jews to 16q24Almogit Abu, Moshe Frydman, Dina Marek, et al.
Journal of Applied Genetics|May 18, 2011
X inactivation testing for identifying a non-syndromic X-linked mental retardation geneHagith Yonath, Dina Marek-Yagel, Haike Resnik-Wolf, et al.
Human Mutation|March 17, 2004
Genetic and biochemical analyses of Israeli osteogenesis imperfecta patientsLiat Ries-Levavi, Tsofia Ish-Shalom, Moshe Frydman, et al.
American Journal of Human Genetics|March 28, 2002
A missense mutation in the LIM2 gene is associated with autosomal recessive presenile cataract in an inbred Iraqi Jewish familyEran Pras, Etgar Levy-Nissenbaum, Tangiz Bakhan, et al.
Archives of Otolaryngology--Head & Neck Surgery|May 17, 2006
Connexin-associated deafness and speech perception outcome of cochlear implantationRiki Taitelbaum-Swead, Zippora Brownstein, Chava Muchnik, et al.
Pageof 5