| Title | Author(s) | Year | View Count |
 | Mutation analysis for heterozygote detection and the prenatal diagnosis of cystic fibrosis | Lemna, WK; Feldman, GL; Kerem, B; Fernbach, SD; Zevkovich, EP; O'Brien, WE; Riordan, JR; Collins, FS; Tsui, LC; Beaudet, AL | 1990 | 363 |
| Mutation analysis in cystic fibrosis (I: Reply) | Lemna, WK; Feldman, GL; Fernbach, SD; Zevkovich, EP; O'Brien, WE; Beaudet, AL; Collins, FS; Kerem, BS; Riordan, JR; Tsui, LC | 1990 | 108 |
 | DNA amplification for detection of the XV-2c polymorphism linked to cystic fibrosis | Rosenbloom, CL; Kerem, BS; Rommens, JM; Tsui, LC; Wainwright, B; Williamson, R; O'Brien, WE; Beaudet, AL | 1989 | 127 |
| Unusual segregation of cystic fibrosis alleles [6] | Kitzis, A; Chomel, JC; Haliassos, A; Tesson, L; Kaplan, JC; Feingold, J; Giraud, G; Labbe, A; Dastugue, B; Dumur, V; Farriaux, JP; Roussel, P; Ferrec, C; Vidaud, M; Goossens, M; Bozon, D; Auvinet, M; Chambon, V; Andre, J; Lissens, W; Bonduelle, M; Liebaers, I; Cochaux, P; Vassart, G; Willems, P; DuckworthRaysiecki, G; Kerem, BS; Tsui, LC; Ray, PN; Krawczak, M; Schmidtke, J; Novelli, G; Dallapiccola, B; Gasparni, G; Pignatti, PP; Seia, M; Ferrari, M; Devoto, M; Romeo, G; Schwarz, M; Super, M; Ivinson, A; Read, AP; Meredith, L; Curtis, A; Williamson, R; Beaudet, AL; Feldman, GL; O'Brien, WE; Bowcock, AM; CavalliSforza, LL; Gilbert, F; Braman, J; King, MC | 1988 | 93 |
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