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K Klinger

Showing results (21-30 of 33) with videos related to

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Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 1, 1992
Molecular analysis of human chromosome 16 cosmid clones containing NotI sitesT Lerner, G Wright, B Leverone, et al.
Human Genetics|August 11, 1992
Incidence and expression of the N1303K mutation of the cystic fibrosis (CFTR) geneL Osborne, G Santis, M Schwarz, et al.
American Journal of Human Genetics|July 1, 1992
Rapid detection of chromosome aneuploidies in uncultured amniocytes by using fluorescence in situ hybridization (FISH)K Klinger, G Landes, D Shook, et al.
Clinical Genetics|April 1, 1996
Maternal origin of transferrin receptor positive cells in venous blood of pregnant womenA Slunga-Tallberg, W el-Rifai, M Keinänen, et al.
Nucleic Acids Research|November 11, 1986
Genetic homogeneity of cystic fibrosisK Klinger, P Stanislovitis, N Hoffman, et al.
American Journal of Human Genetics|December 1, 1986
Linkage of cystic fibrosis to two tightly linked DNA markers: joint report from a collaborative studyA Beaudet, A Bowcock, M Buchwald, 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.
Fetal Diagnosis and Therapy|March 13, 1999
Low false-positive rate of aneuploidy detection using fetal cells isolated from maternal bloodF de la Cruz, H Shifrin, S Elias, 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.
American Journal of Obstetrics and Gynecology|December 1, 1991
Prenatal diagnosis with fetal cells isolated from maternal blood by multiparameter flow cytometryJ O Price, S Elias, S S Wachtel, et al.
Pageof 4

Showing results (21-30 of 33) with videos related to

Sort By:
Pageof 4
Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 1, 1992
Molecular analysis of human chromosome 16 cosmid clones containing NotI sitesT Lerner, G Wright, B Leverone, et al.
Human Genetics|August 11, 1992
Incidence and expression of the N1303K mutation of the cystic fibrosis (CFTR) geneL Osborne, G Santis, M Schwarz, et al.
American Journal of Human Genetics|July 1, 1992
Rapid detection of chromosome aneuploidies in uncultured amniocytes by using fluorescence in situ hybridization (FISH)K Klinger, G Landes, D Shook, et al.
Clinical Genetics|April 1, 1996
Maternal origin of transferrin receptor positive cells in venous blood of pregnant womenA Slunga-Tallberg, W el-Rifai, M Keinänen, et al.
Nucleic Acids Research|November 11, 1986
Genetic homogeneity of cystic fibrosisK Klinger, P Stanislovitis, N Hoffman, et al.
American Journal of Human Genetics|December 1, 1986
Linkage of cystic fibrosis to two tightly linked DNA markers: joint report from a collaborative studyA Beaudet, A Bowcock, M Buchwald, 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.
Fetal Diagnosis and Therapy|March 13, 1999
Low false-positive rate of aneuploidy detection using fetal cells isolated from maternal bloodF de la Cruz, H Shifrin, S Elias, 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.
American Journal of Obstetrics and Gynecology|December 1, 1991
Prenatal diagnosis with fetal cells isolated from maternal blood by multiparameter flow cytometryJ O Price, S Elias, S S Wachtel, et al.
Pageof 4