Fetal gender and aneuploidy detection using fetal cells in maternal blood: analysis of NIFTY I data
Bianchi, D. W., Simpson, J. L., Jackson, L. G., Elias, S., Holzgreve, W., Evans, M. I., Dukes, K. A., Sullivan, L. M., Klinger, K. W., Bischoff, F. Z., Hahn, S., Johnson, K. L., Lewis, D., Wapner, R. J., Cruz, F. de la
Published in Prenatal diagnosis (01.07.2002)
Published in Prenatal diagnosis (01.07.2002)
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PCR quantitation of fetal cells in maternal blood in normal and aneuploid pregnancies
BIANCHI, D. W, WILLIAMS, J. M, SULLIVAN, L. M, HANSON, F. W, KLINGER, K. W, SHUBER, A. P
Published in American journal of human genetics (01.10.1997)
Published in American journal of human genetics (01.10.1997)
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Strong homophilic interactions of the Ig-like domains of polycystin-1, the protein product of an autosomal dominant polycystic kidney disease gene, PKD1
IBRAGHIMOV-BESKROVNAYA, O, BUKANOV, N. O, DONOHUE, L. C, DACKOWSKI, W. R, KLINGER, K. W, LANDES, G. M
Published in Human molecular genetics (01.07.2000)
Published in Human molecular genetics (01.07.2000)
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Mutation Detection of PKD1 Identifies a Novel Mutation Common to Three Families with Aneurysms and/or Very-Early-Onset Disease
Watnick, Terry, Phakdeekitcharoen, Bunyong, Johnson, Ann, Gandolph, Michael, Wang, Mei, Briefel, Gary, Klinger, Katherine W., Kimberling, William, Gabow, Patricia, Germino, Gregory G.
Published in American journal of human genetics (01.12.1999)
Published in American journal of human genetics (01.12.1999)
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Multiplex PCR amplification from the CFTR gene using DNA prepared from buccal brushes/swabs
Richards, B, Skoletsky, J, Shuber, A P, Balfour, R, Stern, R C, Dorkin, H L, Parad, R B, Witt, D, Klinger, K W
Published in Human molecular genetics (01.02.1993)
Published in Human molecular genetics (01.02.1993)
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High Throughput Parallel Analysis of Hundreds of Patient Samples for More Than 100 Mutations in Multiple Disease Genes
Shuber, Anthony P., Michalowsky, Lesley A., Scott Nass, G., Skoletsky, Joel, Hire, Lisa M., Kotsopoulos, Steve K., Phipps, Michael F., Barberio, Dana M., Klinger, Katherine W.
Published in Human molecular genetics (01.03.1997)
Published in Human molecular genetics (01.03.1997)
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Expression of cystic fibrosis transmembrane conductance regulator corrects defective chloride channel regulation in cystic fibrosis airway epithelial cells
Rich, Devra P, Anderson, Matthew P, Gregory, Richard J, Cheng, Seng H, Paul, Sucharita, Jefferson, Douglas M, McCann, John D, Klinger, Katherine W, Smith, Alan E, Welsh, Michael J
Published in Nature (London) (27.09.1990)
Published in Nature (London) (27.09.1990)
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Expression and characterization of the cystic fibrosis transmembrane conductance regulator
Gregory, Richard J, Cheng, Seng H, Rich, Devra P, Marshall, John, Paul, Sucharita, Hehir, Kathleen, Ostedgaard, Lynda, Klinger, Katherine W, Welsh, Michael J, Smith, Alan E
Published in Nature (London) (27.09.1990)
Published in Nature (London) (27.09.1990)
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Prenatal detection of chromosome aneuploidies in uncultured chorionic villus samples by FISH
BRYNDORF, T, CHRISTENSEN, B, VAD, M, PARNER, J, CARELLI, M. P, WARD, B. E, KLINGER, K. W, BANG, J, PHILIP, J
Published in American journal of human genetics (01.10.1996)
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Published in American journal of human genetics (01.10.1996)
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Transcriptional response to GAA deficiency (Pompe disease) in infantile-onset patients
Palermo, A.T., Palmer, R.E., So, K.S., Oba-Shinjo, S.M., Zhang, M., Richards, B., Madhiwalla, S.T., Finn, P.F., Hasegawa, A., Ciociola, K.M., Pescatori, M., McVie-Wylie, A.J., Mattaliano, R.J., Madden, S.L., Marie, S.K.N., Klinger, K.W., Pomponio, R.J.
Published in Molecular genetics and metabolism (01.07.2012)
Published in Molecular genetics and metabolism (01.07.2012)
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Plasminogen Activator Inhibitor Type 1 Gene is Located at Region q21.3-q22 of Chromosome 7 and Genetically Linked with Cystic Fibrosis
Klinger, K. W., Winqvist, R., Riccio, A., Andreasen, P. A., Sartorio, R., Nielsen, L. S., Stuart, N., Stanislovitis, P., Watkins, P., Douglas, R., K.-H. Grzeschik, Alitalo, K., Blasi, F., Danø, K.
Published in Proceedings of the National Academy of Sciences - PNAS (01.12.1987)
Published in Proceedings of the National Academy of Sciences - PNAS (01.12.1987)
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Fetal cells in maternal blood: Determination of purity and yield by quantitative polymerase chain reaction
Bianchi, Diana W., Shuber, Anthony P., DeMaria, Mary Ann, Fougner, Arthur C., Klinger, Katherine W.
Published in American journal of obstetrics and gynecology (01.10.1994)
Published in American journal of obstetrics and gynecology (01.10.1994)
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Conference Proceeding
Expression of normal and cystic fibrosis phenotypes by continuous airway epithelial cell lines
Jefferson, D M, Valentich, J D, Marini, F C, Grubman, S A, Iannuzzi, M C, Dorkin, H L, Li, M, Klinger, K W, Welsh, M J
Published in The American journal of physiology (01.12.1990)
Published in The American journal of physiology (01.12.1990)
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Detection of fetal cells with 47,XY,+21 karyotype in maternal peripheral blood
Bianchi, D W, Mahr, A, Zickwolf, G K, Houseal, T W, Flint, A F, Klinger, K W
Published in Human genetics (01.12.1992)
Published in Human genetics (01.12.1992)
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The NTN2L gene encoding a novel human netrin maps to the autosomal dominant polycystic kidney disease region on chromosome 16p13.3
VAN RAAY, T. J, FOSKETT, S. M, CONNORS, T. D, KLINGER, K. W, LANDES, G. M, BURN, T. C
Published in Genomics (San Diego, Calif.) (15.04.1997)
Published in Genomics (San Diego, Calif.) (15.04.1997)
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Identification of the M1101K mutation in the cystic fibrosis transmembrane conductance regulator (CFTR) gene and complete detection of cystic fibrosis mutations in the hutterite population
ZIELENSKI, J, FUJIWARA, T. M, MARKIEWICZ, D, PARADIS, A. J, ANACLETO, A. I, RICHARDS, B, SCHWARTZ, R. H, KLINGER, K. W, LAP-CHEE TSUI, MORGAN, K
Published in American journal of human genetics (01.03.1993)
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Published in American journal of human genetics (01.03.1993)
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