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American Journal of Human Genetics|November 1, 1987
Linkage of DNA probe B79a (D7S13) to cystic fibrosisB J Wainwright, L C Tsui, M Leppert, et al.Pediatric Research|August 1, 1996
Phenotypic abnormalities in long-term surviving cystic fibrosis miceG Kent, M Oliver, J K Foskett, et al.Proceedings of the National Academy of Sciences of the United States of America|September 13, 1994
Phosphatase inhibitors activate normal and defective CFTR chloride channelsF Becq, T J Jensen, X B Chang, et al.International Journal of Radiation Biology|March 1, 1996
Genetic complementation of radiation response by 3' untranslated regions (UTR) of RNAP Chen, A A Girjes, K Hobson, et al.Nature|November 4, 1985
A polymorphic DNA marker linked to cystic fibrosis is located on chromosome 7R G Knowlton, O Cohen-Haguenauer, N Van Cong, et al.Somatic Cell and Molecular Genetics|March 1, 1995
Human cDNA clones that modify radiomimetic sensitivity of ataxia-telangiectasia (group A) cellsY Ziv, A Bar-Shira, T J Jorgensen, et al.Proceedings of the National Academy of Sciences of the United States of America|February 7, 1998
Development of an epithelium-specific expression cassette with human DNA regulatory elements for transgene expression in lung airwaysY H Chow, H O'Brodovich, J Plumb, et al.American Journal of Human Genetics|October 23, 1997
Evidence for at least eight Fanconi anemia genesH Joenje, A B Oostra, M Wijker, et al.Blood|September 15, 1995
Classification of Fanconi anemia patients by complementation analysis: evidence for a fifth genetic subtypeH Joenje, J R Lo ten Foe, A B Oostra, et al.Genomics|April 11, 2000
The human homolog of insect-derived growth factor, CECR1, is a candidate gene for features of cat eye syndromeM A Riazi, P Brinkman-Mills, T Nguyen, et al.Pageof 15