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American Journal of Human Genetics|December 1, 1986
A linkage study of cystic fibrosis in extended multigenerational pedigreesP C Watkins, R Schwartz, N Hoffman, et al.American Journal of Human Genetics|May 1, 1990
Cystic fibrosis mutations in the Hutterite BrethrenK Klinger, G T Horn, P Stanislovitis, et al.Cytogenetics and Cell Genetics|January 1, 1991
Deletion mapping of plasminogen activator inhibitor, type I (PLANH1) and beta-glucuronidase (GUSB) in 7q21----q22C E Schwartz, P Stanislovitis, M C Phelan, et al.Nucleic Acids Research|November 11, 1986
Genetic homogeneity of cystic fibrosisK Klinger, P Stanislovitis, N Hoffman, et al.Proceedings of the National Academy of Sciences of the United States of America|December 1, 1987
Plasminogen activator inhibitor type 1 gene is located at region q21.3-q22 of chromosome 7 and genetically linked with cystic fibrosisK W Klinger, R Winqvist, A Riccio, et al.Cytogenetics and Cell Genetics|January 1, 1986
Regional assignment of the erythropoietin gene to human chromosome region 7pter----q22P C Watkins, R Eddy, N Hoffman, et al.American Journal of Human Genetics|March 1, 1989
Genealogical analysis of cystic fibrosis families and chromosome 7q RFLP haplotypes in the Hutterite BrethrenT M Fujiwara, K Morgan, R H Schwartz, 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.Pageof 1