| Title | Author(s) | Year | View Count |
 | Absence of a paternally inherited FOXP2 gene in developmental verbal dyspraxia | Feuk, L; Kalervo, A; LipsanenNyman, M; Skaug, J; Nakabayashi, K; Finucane, B; Hartung, D; Innes, M; Kerem, B; Nowaczyk, MJ; Rivlin, J; Roberts, W; Senman, L; Summers, A; Szatmari, P; Wong, V; Vincent, JB; Zeesman, S; Osborne, LR; Cardy, JO; Kere, J; Scherer, SW; HannulaJouppi, K | 2006 | 462 |
 | Human chromosome 7: DNA sequence and biology | Scherer, SW; Cheung, J; MacDonald, JR; Osborne, LR; Nakabayashi, K; Herbrick, JA; Carson, AR; ParkerKatiraee, L; Skaug, J; Khaja, R; Zhang, J; Hudek, AK; Li, M; Haddad, M; Duggan, GE; Fernandez, BA; Kanematsu, E; Gentles, S; Christopoulos, CC; Choufani, S; Kwasnicka, D; Zheng, XH; Lai, Z; Nusskern, D; Zhang, Q; Gu, Z; Lu, F; Zeesman, S; Nowaczyk, MJ; Teshima, I; Chitayat, D; Shuman, C; Weksberg, R; Zackai, EH; Grebe, TA; Cox, SR; Kirkpatrick, SJ; Rahman, N; Friedman, JM; Heng, HHQ; Pelicci, PG; LoCoco, F; Belloni, E; Shaffer, LG; Pober, B; Morton, CC; Gusella, JF; Bruns, GAP; Korf, BR; Quade, BJ; Ligon, AH; Ferguson, H; Higgins, AW; Leach, NT; Herrick, SR; Lemyre, E; Farra, CG; Kim, HG; Summers, AM; Gripp, KW; Roberts, W; Szatmari, P; Winsor, EJT; Grzeschik, KH; Teebi, A; Minassian, BA; Kere, J; Armengol, L; Pujana, MA; Estivill, X; Wilson, MD; Koop, BF; Tosi, S; Moore, GE; Boright, AP; Zlotorynski, E; Kerem, B; Kroisel, PM; Petek, E; Oscier, DG; Mould, SJ; Döhner, H; Döhner, K; Rommens, JM; Vincent, JB; Venter, JC; Li, PW; Mural, RJ; Adams, MD; Tsui, LC | 2003 | 679 |
| Replication delay along FRA7H, a common fragile site on human chromosome 7, leads to chromosomal instability | Hellman, A; Rahat, A; Scherer, SW; Darvasi, A; Tsui, LC; Kerem, B | 2000 | 379 |
| Molecular characterization of a common fragile site (FRA7H) on human chromosome 7 by the cloning of a simian virus 40 integration site | Mishmar, D; Rahat, A; Scherer, SW; Nyakatura, G; Hinzmann, B; Kohwi, Y; MandelGutfroind, Y; Lee, JR; Drescher, B; Sas, DE; Margalit, H; Platzer, M; Weiss, A; Tsui, LC; Rosenthal, A; Kerem, B | 1998 | 1,267 |
| 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 |
 | Methods for analysis of multiple cystic fibrosis mutations | Ng, ISL; Pace, R; Richard, MV; Kobayashi, K; Kerem, B; Tsui, LC; Beaudet, AL | 1991 | 227 |
| Identification of mutations in regions corresponding to the two putative nucleotide (ATP)-binding folds of the cystic fibrosis gene | Kerem, B; Zielenski, J; Markiewicz, D; Bozon, D; Gazit, E; Yahav, J; Kennedy, D; Riordan, JR; Collins, FS; Rommens, JM; Tsui, LC | 1990 | 299 |
| 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 |
| Clinical and genetic comparisons of patients with cystic fibrosis, with or without meconium ileus | Kerem, E; Corey, M; Kerem, B; Durie, P; Tsui, LC; Levison, H | 1989 | 255 |
| Identification and regional localization of DNA markers on chromosome 7 for the cloning of the cystic fibrosis gene | Rommens, JM; Zengerling, S; Burns, J; Melmer, G; Kerem, B; Plavsic, N; Zsiga, M; Kennedy, D; Markiewicz, D; Rozmahel, R; Riordan, JR; Buchwald, M; Tsui, L | 1988 | 255 |
| Methods Of Detecting Cystic Fibrosis Gene By Nucleic Acid Hybridization | Tsui, L-C; Riordan, JR; Rommens, JM; Kerem, B; Buchwald, M; Collins, FS; Iannuzzi, M; Drumm, M | - | 507 |
| Methods For Screening For Mutations At Various Positions In The Introns And Exons Of The Cystic Fibrosis Gene | Tsui, L-C; Rommens, JR; Kerem, B | - | 589 |
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