| Title | Author(s) | Year | View Count |
 | Cystic fibrosis patients bearing both the common missense mutation Gly→Asp at codon 551 and the ΔF508 mutation are clinically indistinguishable from ΔF508 homozygotes, except for decreased risk of meconium ileus | Hamosh, A; King, TM; Rosenstein, BJ; Corey, M; Levison, H; Durie, P; Tsui , LC; Mcintosh, I; Keston, M; Brock, DJH; Macek Jr, M; Zemkova, D; Krasnicanova, H; Vavrova, V; Macek Sr, M; Golder, N; Schwarz, MJ; Super, M; Watson, EK | 1992 | 28 |
| 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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