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B Kerem

Showing results (11-20 of 44) with videos related to

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Annals of Human Biology|March 5, 2002
Protein electrophoretic markers in Israel: compilation of data and genetic affinitiesA Zoossmann-Diskin, A Joel, M Liron, et al.
American Journal of Medical Genetics|February 1, 1991
Endoreduplication and polyploidy in fragile X cells induced by methotrexate and fluorodeoxyuridine: implications for diagnosisC Kimchi-Sarfaty, R Goitein, B Kerem, et al.
The Journal of Pediatrics|May 1, 1989
Clinical and genetic comparisons of patients with cystic fibrosis, with or without meconium ileusE Kerem, M Corey, B Kerem, et al.
Molecular and Cellular Biology|May 29, 2000
Replication delay along FRA7H, a common fragile site on human chromosome 7, leads to chromosomal instabilityA Hellman, A Rahat, S W Scherer, et al.
Circulation|April 12, 2000
Effects of flecainide in patients with new SCN5A mutation: mutation-specific therapy for long-QT syndrome?J Benhorin, R Taub, M Goldmit, et al.
American Journal of Human Genetics|December 1, 1989
Physical localization of two DNA markers closely linked to the cystic fibrosis locus by pulsed-field gel electrophoresisJ M Rommens, S Zengerling-Lentes, B Kerem, et al.
Genomics|May 1, 1991
Identification of mutations in exons 1 through 8 of the cystic fibrosis transmembrane conductance regulator (CFTR) geneJ Zielenski, D Bozon, B Kerem, et al.
European Journal of Human Genetics : EJHG|October 22, 1998
Screening of CFTR mutations in an isolated population: identification of carriers and patientsO Chiba-Falek, M Nissim-Rafinia, Z Argaman, et al.
Journal of Learning Disabilities|October 23, 2004
Developmental dyscalculia is a familial learning disabilityR S Shalev, O Manor, B Kerem, et al.
Cytogenetics and Cell Genetics|July 25, 1998
An interstitial nucleolus organizer region in the long arm of human chromosome 7: cytogenetic characterization and familial segregationM Guttenbach, N Nassar, W Feichtinger, et al.
Pageof 5

Showing results (11-20 of 44) with videos related to

Sort By:
Pageof 5
Annals of Human Biology|March 5, 2002
Protein electrophoretic markers in Israel: compilation of data and genetic affinitiesA Zoossmann-Diskin, A Joel, M Liron, et al.
American Journal of Medical Genetics|February 1, 1991
Endoreduplication and polyploidy in fragile X cells induced by methotrexate and fluorodeoxyuridine: implications for diagnosisC Kimchi-Sarfaty, R Goitein, B Kerem, et al.
The Journal of Pediatrics|May 1, 1989
Clinical and genetic comparisons of patients with cystic fibrosis, with or without meconium ileusE Kerem, M Corey, B Kerem, et al.
Molecular and Cellular Biology|May 29, 2000
Replication delay along FRA7H, a common fragile site on human chromosome 7, leads to chromosomal instabilityA Hellman, A Rahat, S W Scherer, et al.
Circulation|April 12, 2000
Effects of flecainide in patients with new SCN5A mutation: mutation-specific therapy for long-QT syndrome?J Benhorin, R Taub, M Goldmit, et al.
American Journal of Human Genetics|December 1, 1989
Physical localization of two DNA markers closely linked to the cystic fibrosis locus by pulsed-field gel electrophoresisJ M Rommens, S Zengerling-Lentes, B Kerem, et al.
Genomics|May 1, 1991
Identification of mutations in exons 1 through 8 of the cystic fibrosis transmembrane conductance regulator (CFTR) geneJ Zielenski, D Bozon, B Kerem, et al.
European Journal of Human Genetics : EJHG|October 22, 1998
Screening of CFTR mutations in an isolated population: identification of carriers and patientsO Chiba-Falek, M Nissim-Rafinia, Z Argaman, et al.
Journal of Learning Disabilities|October 23, 2004
Developmental dyscalculia is a familial learning disabilityR S Shalev, O Manor, B Kerem, et al.
Cytogenetics and Cell Genetics|July 25, 1998
An interstitial nucleolus organizer region in the long arm of human chromosome 7: cytogenetic characterization and familial segregationM Guttenbach, N Nassar, W Feichtinger, et al.
Pageof 5