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Y Yahav

Showing results (21-30 of 38) with videos related to

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Harefuah|December 15, 1995
[Neurological symptoms associated with vitamin E deficiency]B A Sela, Z Shorer, R Doolman, et al.
Pediatrics|December 1, 1992
Cystic fibrosis manifested as undescended testis and absence of vas deferensR Goshen, E Kerem, T Shoshani, et al.
Respiration; International Review of Thoracic Diseases|January 1, 1989
Immediate effect of various treatments on lung function in infants with cystic fibrosisC Maayan, E Bar-Yishay, T Yaacobi, et al.
Harefuah|April 15, 1979
[Complications of heart catheterization in infants and children]H Kaplinsky, Y Yahav, A Shem Tov, et al.
The Journal of Clinical Investigation|April 1, 1994
Similar levels of mRNA from the W1282X and the delta F508 cystic fibrosis alleles, in nasal epithelial cellsT Shoshani, E Kerem, A Szeinberg, et al.
American Journal of Human Genetics|January 1, 1992
Association of a nonsense mutation (W1282X), the most common mutation in the Ashkenazi Jewish cystic fibrosis patients in Israel, with presentation of severe diseaseT Shoshani, A Augarten, E Gazit, et al.
Genomics|January 1, 1993
A new mutation in the CFTR gene, composed of two adjacent DNA alterations, is a common cause of cystic fibrosis among Georgian JewsT Shoshani, Y Berkun, Y Yahav, et al.
Lancet (London, England)|November 26, 1994
Congenital bilateral absence of vas deferens in the absence of cystic fibrosisA Augarten, Y Yahav, B S Kerem, et al.
Human Genetics|August 1, 1995
Highly variable incidence of cystic fibrosis and different mutation distribution among different Jewish ethnic groups in IsraelE Kerem, Y M Kalman, Y Yahav, et al.
Lancet (London, England)|July 3, 1993
Mild cystic fibrosis and normal or borderline sweat test in patients with the 3849 + 10 kb C-->T mutationA Augarten, B S Kerem, Y Yahav, et al.
Pageof 4

Showing results (21-30 of 38) with videos related to

Sort By:
Pageof 4
Harefuah|December 15, 1995
[Neurological symptoms associated with vitamin E deficiency]B A Sela, Z Shorer, R Doolman, et al.
Pediatrics|December 1, 1992
Cystic fibrosis manifested as undescended testis and absence of vas deferensR Goshen, E Kerem, T Shoshani, et al.
Respiration; International Review of Thoracic Diseases|January 1, 1989
Immediate effect of various treatments on lung function in infants with cystic fibrosisC Maayan, E Bar-Yishay, T Yaacobi, et al.
Harefuah|April 15, 1979
[Complications of heart catheterization in infants and children]H Kaplinsky, Y Yahav, A Shem Tov, et al.
The Journal of Clinical Investigation|April 1, 1994
Similar levels of mRNA from the W1282X and the delta F508 cystic fibrosis alleles, in nasal epithelial cellsT Shoshani, E Kerem, A Szeinberg, et al.
American Journal of Human Genetics|January 1, 1992
Association of a nonsense mutation (W1282X), the most common mutation in the Ashkenazi Jewish cystic fibrosis patients in Israel, with presentation of severe diseaseT Shoshani, A Augarten, E Gazit, et al.
Genomics|January 1, 1993
A new mutation in the CFTR gene, composed of two adjacent DNA alterations, is a common cause of cystic fibrosis among Georgian JewsT Shoshani, Y Berkun, Y Yahav, et al.
Lancet (London, England)|November 26, 1994
Congenital bilateral absence of vas deferens in the absence of cystic fibrosisA Augarten, Y Yahav, B S Kerem, et al.
Human Genetics|August 1, 1995
Highly variable incidence of cystic fibrosis and different mutation distribution among different Jewish ethnic groups in IsraelE Kerem, Y M Kalman, Y Yahav, et al.
Lancet (London, England)|July 3, 1993
Mild cystic fibrosis and normal or borderline sweat test in patients with the 3849 + 10 kb C-->T mutationA Augarten, B S Kerem, Y Yahav, et al.
Pageof 4