Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

N Magal

Showing results (21-30 of 30) with videos related to

Pageof 3
Sort By:
You have reached the last page of results.This site can display upto 30 results.
Clinical Genetics|May 1, 2008
Autosomal recessive ichthyosis with hypotrichosis syndrome: further delineation of the phenotypeL Avrahami, S Maas, M Pasmanik-Chor, et al.
American Journal of Human Genetics|July 10, 2001
Fragile-X carrier screening and the prevalence of premutation and full-mutation carriers in IsraelH Toledano-Alhadef, L Basel-Vanagaite, N Magal, et al.
American Journal of Human Genetics|December 1, 1992
The gene for familial Mediterranean fever in both Armenians and non-Ashkenazi Jews is linked to the alpha-globin complex on 16p: evidence for locus homogeneityM Shohat, X Bu, T Shohat, et al.
Clinical Genetics|January 11, 2014
Founder mutation for Huntington disease in Caucasus JewsO Melamed, D M Behar, C Bram, et al.
Clinical Genetics|June 24, 2011
High frequency of autosomal-recessive DFNB59 hearing loss in an isolated Arab population in IsraelG Borck, L Rainshtein, S Hellman-Aharony, et al.
Pediatrics|May 9, 2000
Familial Mediterranean fever: effects of genotype and ethnicity on inflammatory attacks and amyloidosisA Mimouni, N Magal, N Stoffman, et al.
Molecular Genetics and Metabolism|December 16, 1998
Amyloidosis in familial mediterranean fever is associated with a specific ancestral haplotype in the MEFV locusM Shohat, R Lotan, N Magal, et al.
European Journal of Human Genetics : EJHG|May 11, 1999
Phenotype-genotype correlation in familial Mediterranean fever: evidence for an association between Met694Val and amyloidosisM Shohat, N Magal, T Shohat, et al.
Journal of Medical Genetics|July 22, 2005
The CC2D1A, a member of a new gene family with C2 domains, is involved in autosomal recessive non-syndromic mental retardationL Basel-Vanagaite, R Attia, M Yahav, et al.
Human Mutation|September 23, 1998
Prevalence of glucocerebrosidase mutations in the Israeli Ashkenazi Jewish populationM Horowitz, M Pasmanik-Chor, Z Borochowitz, et al.
Pageof 3

Showing results (21-30 of 30) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 30 results.
Clinical Genetics|May 1, 2008
Autosomal recessive ichthyosis with hypotrichosis syndrome: further delineation of the phenotypeL Avrahami, S Maas, M Pasmanik-Chor, et al.
American Journal of Human Genetics|July 10, 2001
Fragile-X carrier screening and the prevalence of premutation and full-mutation carriers in IsraelH Toledano-Alhadef, L Basel-Vanagaite, N Magal, et al.
American Journal of Human Genetics|December 1, 1992
The gene for familial Mediterranean fever in both Armenians and non-Ashkenazi Jews is linked to the alpha-globin complex on 16p: evidence for locus homogeneityM Shohat, X Bu, T Shohat, et al.
Clinical Genetics|January 11, 2014
Founder mutation for Huntington disease in Caucasus JewsO Melamed, D M Behar, C Bram, et al.
Clinical Genetics|June 24, 2011
High frequency of autosomal-recessive DFNB59 hearing loss in an isolated Arab population in IsraelG Borck, L Rainshtein, S Hellman-Aharony, et al.
Pediatrics|May 9, 2000
Familial Mediterranean fever: effects of genotype and ethnicity on inflammatory attacks and amyloidosisA Mimouni, N Magal, N Stoffman, et al.
Molecular Genetics and Metabolism|December 16, 1998
Amyloidosis in familial mediterranean fever is associated with a specific ancestral haplotype in the MEFV locusM Shohat, R Lotan, N Magal, et al.
European Journal of Human Genetics : EJHG|May 11, 1999
Phenotype-genotype correlation in familial Mediterranean fever: evidence for an association between Met694Val and amyloidosisM Shohat, N Magal, T Shohat, et al.
Journal of Medical Genetics|July 22, 2005
The CC2D1A, a member of a new gene family with C2 domains, is involved in autosomal recessive non-syndromic mental retardationL Basel-Vanagaite, R Attia, M Yahav, et al.
Human Mutation|September 23, 1998
Prevalence of glucocerebrosidase mutations in the Israeli Ashkenazi Jewish populationM Horowitz, M Pasmanik-Chor, Z Borochowitz, et al.
Pageof 3