| Title | Author(s) | Year | View Count |
 | Identification of genes from a 500-kb region at 7q11.23 that is commonly deleted in Williams syndrome patients | Osborne, LR; Martindale, D; Scherer, SW; Shi, XM; Huizenga, J; Heng, HHQ; Costa, T; Pober, B; Lew, L; Brinkman, J; Rommens, J; Koop, B; Tsui, LC | 1996 | 288 |
 | Genetic determination of exocrine pancreatic function in cystic fibrosis | Kristidis, P; Bozon, D; Corey, M; Markiewicz, D; Rommens, J; Tsui, LC; Durie, P | 1992 | 264 |
 | Molecular genetics of cystic fibrosis | Tsui, LC; Rommens, J; Kerem, B; Rozmahel, R; Zielenski, J; Kennedy, D; Markiewicz, D; Plavsic, N; Chou, JL; Bozon, D; Dobbs, M | 1991 | 115 |
| Genomic DNA sequence of the cystic fibrosis transmembrane conductance regulator (CFTR) gene | Zielenski, J; Rozmahel, R; Bozon, D; Kerem, BS; Grzelczak, Z; Riordan, JR; Rommens, J; Tsui, LC | 1991 | 301 |
| A cluster of highly polymorphic dinucleotide repeats in intron 17b of the cystic fibrosis transmembrane conductance regulator (CFTR) gene | Zielenski, J; Markiewicz, D; Rininsland, F; Rommens, J; Tsui, LC | 1991 | 331 |
| Isolation of clones on chromosome 7 that contain recognition sites for rare-cutting enzymes by oligonucleotide hybridization | Melmer, G; Sood, R; Rommens, J; Rego, D; Tsui, LC; Buchwald, M | 1990 | 269 |
| Rapid nonradioactive detection of the major cystic fibrosis mutation | Rommens, J; Keram, BS; Greer, W; Chang, P; Tsui, LC; Ray, P | 1990 | 263 |
| 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, P | 1990 | 379 |
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