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N Magal

Showing results (11-20 of 30) with videos related to

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Molecular Psychiatry|March 24, 1999
A novel allele in the promoter region of the human serotonin transporter geneE Michaelovsky, A Frisch, R Rockah, et al.
Journal of Clinical Gastroenterology|July 2, 1998
Abnormal liver test results in myotonic dystrophyA Achiron, Y Barak, N Magal, et al.
Journal of Medical Genetics|October 22, 2003
Mapping of a new locus for autosomal recessive non-syndromic mental retardation in the chromosomal region 19p13.12-p13.2: further genetic heterogeneityL Basel-Vanagaite, A Alkelai, R Straussberg, et al.
Seminars in Arthritis and Rheumatism|November 9, 2000
Renal outcome and vascular morbidity in systemic lupus erythematosus (SLE): lack of association with the angiotensin-converting enzyme gene polymorphismY Molad, E Gal, N Magal, et al.
American Journal of Human Genetics|November 5, 1997
A gene for arthrogryposis multiplex congenita neuropathic type is linked to D5S394 on chromosome 5qterM Shohat, R Lotan, N Magal, et al.
The Israel Medical Association Journal : IMAJ|January 17, 2002
Autosomal dominant nephritis with renal failure of non-Alport type: clinical and molecular studiesT Ilan, T Shohat, A Tobar, et al.
American Journal of Medical Genetics|June 27, 2000
Increased transmission of intermediate alleles of the FMR1 gene compared with normal alleles among female heterozygotesV Drasinover, S Ehrlich, N Magal, et al.
Neurology|January 14, 2004
Infantile bilateral striatal necrosis maps to chromosome 19qL Basel-Vanagaite, R Straussberg, H Ovadia, et al.
Clinical Genetics|March 21, 2017
Mutations in ERGIC1 cause Arthrogryposis multiplex congenita, neuropathic typeE Reinstein, V Drasinover, R Lotan, et al.
European Journal of Human Genetics : EJHG|June 15, 2000
Higher than expected carrier rates for familial Mediterranean fever in various Jewish ethnic groupsN Stoffman, N Magal, T Shohat, et al.
Pageof 3

Showing results (11-20 of 30) with videos related to

Sort By:
Pageof 3
Molecular Psychiatry|March 24, 1999
A novel allele in the promoter region of the human serotonin transporter geneE Michaelovsky, A Frisch, R Rockah, et al.
Journal of Clinical Gastroenterology|July 2, 1998
Abnormal liver test results in myotonic dystrophyA Achiron, Y Barak, N Magal, et al.
Journal of Medical Genetics|October 22, 2003
Mapping of a new locus for autosomal recessive non-syndromic mental retardation in the chromosomal region 19p13.12-p13.2: further genetic heterogeneityL Basel-Vanagaite, A Alkelai, R Straussberg, et al.
Seminars in Arthritis and Rheumatism|November 9, 2000
Renal outcome and vascular morbidity in systemic lupus erythematosus (SLE): lack of association with the angiotensin-converting enzyme gene polymorphismY Molad, E Gal, N Magal, et al.
American Journal of Human Genetics|November 5, 1997
A gene for arthrogryposis multiplex congenita neuropathic type is linked to D5S394 on chromosome 5qterM Shohat, R Lotan, N Magal, et al.
The Israel Medical Association Journal : IMAJ|January 17, 2002
Autosomal dominant nephritis with renal failure of non-Alport type: clinical and molecular studiesT Ilan, T Shohat, A Tobar, et al.
American Journal of Medical Genetics|June 27, 2000
Increased transmission of intermediate alleles of the FMR1 gene compared with normal alleles among female heterozygotesV Drasinover, S Ehrlich, N Magal, et al.
Neurology|January 14, 2004
Infantile bilateral striatal necrosis maps to chromosome 19qL Basel-Vanagaite, R Straussberg, H Ovadia, et al.
Clinical Genetics|March 21, 2017
Mutations in ERGIC1 cause Arthrogryposis multiplex congenita, neuropathic typeE Reinstein, V Drasinover, R Lotan, et al.
European Journal of Human Genetics : EJHG|June 15, 2000
Higher than expected carrier rates for familial Mediterranean fever in various Jewish ethnic groupsN Stoffman, N Magal, T Shohat, et al.
Pageof 3