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	Title	Author(s)	Issue Date	Views
	Absence of a paternally inherited FOXP2 gene in developmental verbal dyspraxia Journal:American Journal of Human Genetics	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	153
	Clinical and genetic comparisons of patients with cystic fibrosis, with or without meconium ileus Journal:Journal of Pediatrics	Kerem, E Corey, M Kerem, B Durie, P Tsui, LC Levison, H	1989	196
	Human chromosome 7: DNA sequence and biology Journal:Science	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	101
	Identification and regional localization of DNA markers on chromosome 7 for the cloning of the cystic fibrosis gene Journal:American Journal of Human Genetics	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	126
	Identification of mutations in regions corresponding to the two putative nucleotide (ATP)-binding folds of the cystic fibrosis gene Journal:Proceedings of the National Academy of Sciences of the United States of America	Kerem, B Zielenski, J Markiewicz, D Bozon, D Gazit, E Yahav, J Kennedy, D Riordan, JR Collins, FS Rommens, JM Tsui, LC	1990	125
	Methods for analysis of multiple cystic fibrosis mutations Journal:Human Genetics	Ng, ISL Pace, R Richard, MV Kobayashi, K Kerem, B Tsui, LC Beaudet, AL	1991	179
	Molecular characterization of a common fragile site (FRA7H) on human chromosome 7 by the cloning of a simian virus 40 integration site Journal:Proceedings of the National Academy of Sciences of the United States of America	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	133
	Molecular genetics of cystic fibrosis Proceeding/Conference:Advances in Experimental Medicine and Biology	Tsui, LC Rommens, J Kerem, B Rozmahel, R Zielenski, J Kennedy, D Markiewicz, D Plavsic, N Chou, JL Bozon, D Dobbs, M	1991	135
	Mutation analysis for heterozygote detection and the prenatal diagnosis of cystic fibrosis Journal:New England Journal of Medicine	Lemna, WK Feldman, GL Kerem, B Fernbach, SD Zevkovich, EP O'Brien, WE Riordan, JR Collins, FS Tsui, LC Beaudet, AL	1990	143
	Replication delay along FRA7H, a common fragile site on human chromosome 7, leads to chromosomal instability Journal:Molecular and Cellular Biology	Hellman, A Rahat, A Scherer, SW Darvasi, A Tsui, LC Kerem, B	2000	133

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