P. Stanislovitis

A linkage study of cystic fibrosis in extended multigenerational pedigrees.

K. Klinger, R. Schwartz, R. Doherty, 1986, American journal of human genetics.

Three RFLPs are detected by an alpha spectrin genomic clone.

K. Klinger, A. Linnenbach, B. Forget, 1987, Nucleic acids research.

Regional assignment of the erythropoietin gene to human chromosome region 7pter----q22.

R. Eddy, T. Shows, J. Gusella, 1986, Cytogenetics and cell genetics.

Plasminogen activator inhibitor type 1 gene is located at region q21.3-q22 of chromosome 7 and genetically linked with cystic fibrosis.

K. Klinger, R. Winqvist, P. Andreasen, 1987, Proceedings of the National Academy of Sciences of the United States of America.

Cystic fibrosis mutations in the Hutterite Brethren.

K. Klinger, R. Schwartz, K. Morgan, 1990, American journal of human genetics.

Genealogical analysis of cystic fibrosis families and chromosome 7q RFLP haplotypes in the Hutterite Brethren.

K. Klinger, R. Schwartz, K. Morgan, 1989, American journal of human genetics.

Cystic fibrosis mutations in North American populations of French ancestry: analysis of Quebec French-Canadian and Louisiana Acadian families.

K. Klinger, L. Tsui, B. Kerem, 1990, American Journal of Human Genetics.

Molecular and genetic analyses at the CF locus.

K. Klinger, P. Stanislovitis, G. Horn, 1991, Advances in experimental medicine and biology.