Results 1 to 8 of 8
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TypeTitleAuthor(s)YearViews
Identification of genes from a 500-kb region at 7q11.23 that is commonly deleted in Williams syndrome patientsOsborne, LR; Martindale, D; Scherer, SW; Shi, XM; Huizenga, J; Heng, HHQ; Costa, T; Pober, B; Lew, L; Brinkman, J; Rommens, J; Koop, B; Tsui, LC1996284
 
Genetic determination of exocrine pancreatic function in cystic fibrosisKristidis, P; Bozon, D; Corey, M; Markiewicz, D; Rommens, J; Tsui, LC; Durie, P1992249
 
Molecular genetics of cystic fibrosisTsui, LC; Rommens, J; Kerem, B; Rozmahel, R; Zielenski, J; Kennedy, D; Markiewicz, D; Plavsic, N; Chou, JL; Bozon, D; Dobbs, M1991149
 
A cluster of highly polymorphic dinucleotide repeats in intron 17b of the cystic fibrosis transmembrane conductance regulator (CFTR) geneZielenski, J; Markiewicz, D; Rininsland, F; Rommens, J; Tsui, LC1991301
 
Genomic DNA sequence of the cystic fibrosis transmembrane conductance regulator (CFTR) geneZielenski, J; Rozmahel, R; Bozon, D; Kerem, BS; Grzelczak, Z; Riordan, JR; Rommens, J; Tsui, LC1991339
 
Isolation of clones on chromosome 7 that contain recognition sites for rare-cutting enzymes by oligonucleotide hybridizationMelmer, G; Sood, R; Rommens, J; Rego, D; Tsui, LC; Buchwald, M1990248
 
The relation between genotype and phenotype in cystic fibrosis - Analysis of the most common mutation (ΔF 508)Kerem, E; Corey, M; Kerem, BS; Rommens, J; Markiewicz, D; Levison, H; Tsui, LC; Durie, P1990382
 
Rapid nonradioactive detection of the major cystic fibrosis mutationRommens, J; Keram, BS; Greer, W; Chang, P; Tsui, LC; Ray, P1990265
 
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