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B Kerem

Showing results (1-10 of 44) with videos related to

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European Journal of Human Genetics : EJHG|January 1, 1995
Deletion and insertion mutations in short tandem repeats in the coding regions of human genesA Darvasi, B Kerem
Current Opinion in Pulmonary Medicine|November 1, 1995
The relationship between genotype and phenotype in cystic fibrosisE Kerem, B Kerem
European Journal of Human Genetics : EJHG|January 1, 1996
The molecular basis for disease variability in cystic fibrosisB Kerem, E Kerem
Chromosoma|January 1, 1988
Cytological evidence of defective template in the fragile X chromosomeB Kerem, R Goitein, T Schaap
Genetic Testing|January 1, 1997
Cystic fibrosis in Jews: frequency and mutation distributionB Kerem, O Chiba-Falek, E Kerem
Oncogene|October 16, 2007
Interplay between ATM and ATR in the regulation of common fragile site stabilityE Ozeri-Galai, M Schwartz, A Rahat, et al.
American Journal of Respiratory and Critical Care Medicine|June 3, 1999
Variable levels of normal RNA in different fetal organs carrying a cystic fibrosis transmembrane conductance regulator splicing mutationO Chiba-Falek, R B Parad, E Kerem, et al.
European Journal of Human Genetics : EJHG|January 1, 1994
Difference in frequencies of the cystic fibrosis alleles, delta F508 and W1282X, between carriers and patientsY M Kalman, E Kerem, A Darvasi, et al.
Circulation|August 23, 2000
Molecular pharmacology of the sodium channel mutation D1790G linked to the long-QT syndromeH Abriel, X H Wehrens, J Benhorin, et al.
Human Molecular Genetics|August 1, 2000
Cellular and viral splicing factors can modify the splicing pattern of CFTR transcripts carrying splicing mutationsM Nissim-Rafinia, O Chiba-Falek, G Sharon, et al.
Pageof 5

Showing results (1-10 of 44) with videos related to

Sort By:
Pageof 5
European Journal of Human Genetics : EJHG|January 1, 1995
Deletion and insertion mutations in short tandem repeats in the coding regions of human genesA Darvasi, B Kerem
Current Opinion in Pulmonary Medicine|November 1, 1995
The relationship between genotype and phenotype in cystic fibrosisE Kerem, B Kerem
European Journal of Human Genetics : EJHG|January 1, 1996
The molecular basis for disease variability in cystic fibrosisB Kerem, E Kerem
Chromosoma|January 1, 1988
Cytological evidence of defective template in the fragile X chromosomeB Kerem, R Goitein, T Schaap
Genetic Testing|January 1, 1997
Cystic fibrosis in Jews: frequency and mutation distributionB Kerem, O Chiba-Falek, E Kerem
Oncogene|October 16, 2007
Interplay between ATM and ATR in the regulation of common fragile site stabilityE Ozeri-Galai, M Schwartz, A Rahat, et al.
American Journal of Respiratory and Critical Care Medicine|June 3, 1999
Variable levels of normal RNA in different fetal organs carrying a cystic fibrosis transmembrane conductance regulator splicing mutationO Chiba-Falek, R B Parad, E Kerem, et al.
European Journal of Human Genetics : EJHG|January 1, 1994
Difference in frequencies of the cystic fibrosis alleles, delta F508 and W1282X, between carriers and patientsY M Kalman, E Kerem, A Darvasi, et al.
Circulation|August 23, 2000
Molecular pharmacology of the sodium channel mutation D1790G linked to the long-QT syndromeH Abriel, X H Wehrens, J Benhorin, et al.
Human Molecular Genetics|August 1, 2000
Cellular and viral splicing factors can modify the splicing pattern of CFTR transcripts carrying splicing mutationsM Nissim-Rafinia, O Chiba-Falek, G Sharon, et al.
Pageof 5