Nonsense mutations accelerate lung disease and decrease survival of cystic fibrosis children von Orenti, Annalisa, Pranke, Iwona, Faucon, Caroline, Varilh, Jessica, Hatton, Aurelie, Golec, Anita, Dehillotte, Clemence, Durieu, Isabelle, Reix, Philippe, Burgel, Pierre-Régis, Grenet, Dominique, Tasset, Céline, Gachelin, Elsa, Perisson, Caroline, Lepissier, Agathe, Dreano, Elise, Tondelier, Danielle, Chevalier, Benoit, Weiss, Laurence, Kiefer, Sébastien, Laurans, Muriel, Chiron, Raphael, Lemonnier, Lydie, Marguet, Christophe, Jung, Andreas, Edelman, Aleksander, Kerem, Bat-Sheva, Girodon, Emmanuelle, Taulan-Cadars, Magali, Hinzpeter, Alexandre, Kerem, Eitan, Naehrlich, Lutz, Sermet-Gaudelus, Isabelle

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The Relation between Genotype and Phenotype in Cystic Fibrosis — Analysis of the Most Common Mutation (ΔF508) von Kerem, Bat-sheva, Kerem, Eitan, Corey, Mary, Rommens, Johanna, Markiewicz, Danuta, Levison, Henry, Tsui, Lap-Chee, Durie, Peter

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Identification of the Cystic Fibrosis Gene: Genetic Analysis von Kerem, Bat-sheva, Rommens, Johanna M., Buchanan, Janet A., Markiewicz, Danuta, Cox, Tara K., Chakravarti, Aravinda, Buchwald, Manuel, Tsui, Lap-Chee

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Identification of the Cystic Fibrosis Gene: Cloning and Characterization of Complementary DNA von Riordan, John R., Rommens, Johanna M., Kerem, Bat-sheva, Alon, Noa, Rozmahel, Richard, Grzelczak, Zbyszko, Zielenski, Julian, Lok, Si, Plavsic, Natasa, Chou, Jia-Ling, Drumm, Mitchell L., Iannuzzi, Michael C., Collins, Francis S., Tsui, Lap-Chee

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Identification of the Cystic Fibrosis Gene: Chromosome Walking and Jumping von Rommens, Johanna M., Iannuzzi, Michael C., Kerem, Bat-sheva, Drumm, Mitchell L., Melmer, Georg, Dean, Michael, Rozmahel, Richard, Cole, Jeffery L., Kennedy, Dara, Hidaka, Noriko, Zsiga, Martha, Buchwald, Manuel, Riordan, John R., Tsui, Lap-Chee, Collins, Francis S.

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Genomic DNA sequence of the cystic fibrosis transmembrane conductance regulator (CFTR) gene von Zielenski, Julian, Rozmahel, Richard, Bozon, Dominique, Kerem, Bat-sheva, Grzelczak, Zbyszko, Riordan, John R., Rommens, Johanna, Tsui, Lap-Chee

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The changing face of the exocrine pancreas in cystic fibrosis: the correlation between pancreatic status, pancreatitis and cystic fibrosis genotype von Augarten, Arie, Tov, Amir Ben, Madgar, Igal, Barak, Asher, Akons, Hanna, Laufer, Joseph, Efrati, Ori, Aviram, Micha, Bentur, Lea, Blau, Hannah, Paret, Gideon, Wilschanski, Michael, Kerem, Bat-Sheva, Yahav, Yaakov

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Identification of mutations in exons 1 through 8 of the cystic fibrosis transmembrane conductance regulator (CFTR) gene von Zielenski, Julian, Bozon, Dominique, Kerem, Bat-sheva, Markiewicz, Danuta, Durie, Peter, Rommens, Johanna M., Tsui, Lap-Chee

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Intra- and extragenic marker haplotypes of CFTR mutations in cystic fibrosis families von DÖRK, T, NEUMANN, T, KLINGER, K, BAT-SHEVA KEREM, ZIELENSKI, J, LAP-CHEE TSUI, TÜMMLER, B, WULBRAND, U, WULF, B, KÄLIN, N, MAASS, G, KRAWCZAK, M, GUILLERMIT, H, FEREC, C, HORN, G

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Identification of Mutations in Regions Corresponding to the Two Putative Nucleotide (ATP)-Binding Folds of the Cystic Fibrosis Gene von Kerem, Bat-sheva, Zielenski, Julian, Markiewicz, Danuta, Bozon, Dominique, Gazit, Ephraim, Yahav, Jacob, Kennedy, Dara, Riordan, John R., Collins, Francis S., Rommens, Johanna M., Tsui, Lap-Chee

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Extended haplotype analysis of cystic fibrosis mutations and its implications for the selective advantage hypothesis von SERETH, H, SHOSHANI, T, NURIT BASHAN, BAT-SHEVA KEREM

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Association of a nonsense mutation (W1282X), the most common mutation in the Ashkenazi Jewish cystic fibrosis patients in Israel, with presentation of severe disease von Shoshani, T, Augarten, A, Gazit, E, Bashan, N, Yahav, Y, Rivlin, Y, Tal, A, Seret, H, Yaar, L, Kerem, E

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Congenital bilateral absence of vas deferens in the absence of cystic fibrosis von Augarten, A., Yahav, Y., Laufer, J., Szeinberg, A., Dor, J., Mashiach, S., Madgar, I., Halle, D., Gazit, E., Kerem, B.S.

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DNA amplification for detection of the XV-2c polymorphism linked to cystic fibrosis von ROSENBLOOM, C. L, BAT-SHEVA KEREM, ROMMENS, J. M, LAP-CHEE TSUI, WAINWRIGHT, B, WILLIAMSON, R, O'BRIEN, W. E, BEAUDET, A. L

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In situ nick-translation distinguishes between active and inactive X chromosomes von Kerem, Bat-Sheva, Goitein, Ruth, Richler, Carmelit, Marcus, Menashe, Cedar, Howard

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Mutation Analysis for Heterozygote Detection and the Prenatal Diagnosis of Cystic Fibrosis von Lemna, Wanda K, Feldman, Gerald L, Kerem, Bat-sheva, Fernbach, Susan D, Zevkovich, Elaine P, O'Brien, William E, Riordan, John R, Collins, Francis S, Tsui, Lap-Chee, Beaudet, Arthur L

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Genetics: Preimplantation diagnosis of cystic fibrosis by simultaneous detection of the W1282X and ΔF508 mutations von Avner, Rachel, Laufer, Neri, Safran, Anat, Kerem, Bat-Sheva, Friedmann, Adam, Mitrani-Rosenbaum, Stella

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Mapping of DNAase I sensitive regions on mitotic chromosomes von Kerem, Bat-Sheva, Goitein, Ruth, Diamond, Gill, Cedar, Howard, Marcus, Menashe

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Methods for analysis of multiple cystic fibrosis mutations von NG, I.S. L, PACE, R, RICHARD, M. V, KOBAYASHI, K, KEREM, B.-S, LAP-CHEE TSUI, BEAUDET, A. L

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Correlation between Genotype and Phenotype in Patients with Cystic Fibrosis von Gan, K H, Heijerman, H G, Bakker, W

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