A macromolecular structure produced by Pseudomonas aeruginosa is recognized by antibody to exotoxin A.

Por Klinger, K W, Shuster, C W
Publicado em 1984

Amplification of a highly polymorphic VNTR segment by the polymerase chain reaction.

Por Horn, G T, Richards, B, Klinger, K W
Publicado em 1989

Alternative splicing of exon 3 of the human growth hormone receptor is the result of an unusual genetic polymorphism.

Por Stallings-Mann, M L, Ludwiczak, R L, Klinger, K W, Rottman, F
Publicado em 1996

Cystic fibrosis mutations in the Hutterite Brethren.

Por Klinger, K, Horn, G T, Stanislovitis, P, Schwartz, R H, Fujiwara, T M, Morgan, K
Publicado em 1990

A linkage study of cystic fibrosis in extended multigenerational pedigrees.

Por Watkins, P C, Schwartz, R, Hoffman, N, Stanislovitis, P, Doherty, R, Klinger, K
Publicado em 1986

Further data on linkage between cystic fibrosis and 7C22 (D7S16)

Por Farrall, M, Lathrop, M, Spence, J E, Bowcock, A, Klinger, K, Tsui, L C
Publicado em 1987

Cystic fibrosis carrier detection using a linked gene probe.

Por Farrall, M, Scambler, P, Klinger, K W, Davies, K, Worrall, C, Williamson, R, Wainwright, B
Publicado em 1986

Three RFLPs are detected by an alpha spectrin genomic clone.

Por Hoffman, N, Stanislovitis, P, Watkins, P C, Klinger, K W, Linnenbach, A J, Forget, B G
Publicado em 1987

Narrowing the position of the Treacher Collins syndrome locus to a small interval between three new microsatellite markers at 5q32-33.1.

Por Dixon, M J, Dixon, J, Houseal, T, Bhatt, M, Ward, D C, Klinger, K, Landes, G M
Publicado em 1993

PCR quantitation of fetal cells in maternal blood in normal and aneuploid pregnancies.

Por Bianchi, D W, Williams, J M, Sullivan, L M, Hanson, F W, Klinger, K W, Shuber, A P
Publicado em 1997

Prenatal detection of chromosome aneuploidies in uncultured chorionic villus samples by FISH.

Por Bryndorf, T., Christensen, B., Vad, M., Parner, J., Carelli, M. P., Ward, B. E., Klinger, K. W., Bang, J., Philip, J.
Publicado em 1996

Genetic homogeneity of cystic fibrosis.

Por Klinger, K, Stanislovitis, P, Hoffman, N, Watkins, P C, Schwartz, R, Doherty, R, Scambler, P, Farrall, M, Williamson, R, Wainwright, B
Publicado em 1986

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

Por Fujiwara, T M, Morgan, K, Schwartz, R H, Doherty, R A, Miller, S R, Klinger, K, Stanislovitis, P, Stuart, N, Watkins, P C
Publicado em 1989

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

Por Klinger, K W, Winqvist, R, Riccio, A, Andreasen, P A, Sartorio, R, Nielsen, L S, Stuart, N, Stanislovitis, P, Watkins, P, Douglas, R
Publicado em 1987

Rapid prenatal diagnosis of chromosomal aneuploidies by fluorescence in situ hybridization: clinical experience with 4,500 specimens.

Por Ward, B E, Gersen, S L, Carelli, M P, McGuire, N M, Dackowski, W R, Weinstein, M, Sandlin, C, Warren, R, Klinger, K W
Publicado em 1993

Identification of the M1101K mutation in the cystic fibrosis transmembrane conductance regulator (CFTR) gene and complete detection of cystic fibrosis mutations in the Hutterite po...

Por Zielenski, J, Fujiwara, T M, Markiewicz, D, Paradis, A J, Anacleto, A I, Richards, B, Schwartz, R H, Klinger, K W, Tsui, L C, Morgan, K
Publicado em 1993

Linkage of cystic fibrosis to two tightly linked DNA markers: Joint report from a collaborative study

Por Beaudet, A., Bowocock, A., Buchwald, M., Cavalli-Sforza, L., Farrall, M., King, M.-C., Klinger, K., Lalouel, J.-M., Lathrop, G., Naylor, S., Ott, J., Tsui, L.-C., Wainwright, B., Watkins, P., White, R., Williamson, R.
Publicado em 1986