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B Kerem

Showing results (31-40 of 44) with videos related to

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Human Mutation|January 8, 2000
Identification of a new SCN5A mutation, D1840G, associated with the long QT syndrome. Mutations in brief no. 153. OnlineJ Benhorin, M Goldmit, J W MacCluer, et al.
Pediatrics|January 26, 1999
Clinical and genetic risk factors for cystic fibrosis-related liver diseaseM Wilschanski, J Rivlin, S Cohen, et al.
Science (New York, N.Y.)|September 8, 1989
Identification of the cystic fibrosis gene: chromosome walking and jumpingJ M Rommens, M C Iannuzzi, B Kerem, et al.
American Journal of Human Genetics|October 1, 1990
Cystic fibrosis mutations in North American populations of French ancestry: analysis of Quebec French-Canadian and Louisiana Acadian familiesR Rozen, R H Schwartz, B C Hilman, et al.
Pediatrics|April 3, 1998
A missense cystic fibrosis transmembrane conductance regulator mutation with variable phenotypeE Kerem, M Nissim-Rafinia, Z Argaman, et al.
Gene Therapy|March 3, 2006
Fragile sites are preferential targets for integrations of MLV vectors in gene therapyA C Bester, M Schwartz, M Schmidt, et al.
Molecular Psychiatry|June 17, 2003
Genome scan of Arab Israeli families maps a schizophrenia susceptibility gene to chromosome 6q23 and supports a locus at chromosome 10q24B Lerer, R H Segman, A Hamdan, et al.
The New England Journal of Medicine|February 1, 1990
Mutation analysis for heterozygote detection and the prenatal diagnosis of cystic fibrosisW K Lemna, G L Feldman, B Kerem, et al.
The European Respiratory Journal|August 9, 2001
Nasal potential difference measurements in patients with atypical cystic fibrosisM Wilschanski, H Famini, N Strauss-Liviatan, et al.
American Journal of Respiratory and Critical Care Medicine|June 1, 1997
A cystic fibrosis transmembrane conductance regulator splice variant with partial penetrance associated with variable cystic fibrosis presentationsE Kerem, N Rave-Harel, A Augarten, et al.
Pageof 5

Showing results (31-40 of 44) with videos related to

Sort By:
Pageof 5
Human Mutation|January 8, 2000
Identification of a new SCN5A mutation, D1840G, associated with the long QT syndrome. Mutations in brief no. 153. OnlineJ Benhorin, M Goldmit, J W MacCluer, et al.
Pediatrics|January 26, 1999
Clinical and genetic risk factors for cystic fibrosis-related liver diseaseM Wilschanski, J Rivlin, S Cohen, et al.
Science (New York, N.Y.)|September 8, 1989
Identification of the cystic fibrosis gene: chromosome walking and jumpingJ M Rommens, M C Iannuzzi, B Kerem, et al.
American Journal of Human Genetics|October 1, 1990
Cystic fibrosis mutations in North American populations of French ancestry: analysis of Quebec French-Canadian and Louisiana Acadian familiesR Rozen, R H Schwartz, B C Hilman, et al.
Pediatrics|April 3, 1998
A missense cystic fibrosis transmembrane conductance regulator mutation with variable phenotypeE Kerem, M Nissim-Rafinia, Z Argaman, et al.
Gene Therapy|March 3, 2006
Fragile sites are preferential targets for integrations of MLV vectors in gene therapyA C Bester, M Schwartz, M Schmidt, et al.
Molecular Psychiatry|June 17, 2003
Genome scan of Arab Israeli families maps a schizophrenia susceptibility gene to chromosome 6q23 and supports a locus at chromosome 10q24B Lerer, R H Segman, A Hamdan, et al.
The New England Journal of Medicine|February 1, 1990
Mutation analysis for heterozygote detection and the prenatal diagnosis of cystic fibrosisW K Lemna, G L Feldman, B Kerem, et al.
The European Respiratory Journal|August 9, 2001
Nasal potential difference measurements in patients with atypical cystic fibrosisM Wilschanski, H Famini, N Strauss-Liviatan, et al.
American Journal of Respiratory and Critical Care Medicine|June 1, 1997
A cystic fibrosis transmembrane conductance regulator splice variant with partial penetrance associated with variable cystic fibrosis presentationsE Kerem, N Rave-Harel, A Augarten, et al.
Pageof 5