Similar articles for PMID: 9683582

Year	Number of Results
1967	1
1968	2
1973	1
1974	2
1976	1
1977	1
1978	1
1982	1
1991	3
1992	5
1993	3
1994	3
1995	3
1996	9
1997	6
1998	6
1999	6
2000	6
2001	6
2003	5
2004	5
2005	2
2006	4
2007	5
2008	4
2009	8
2010	7
2011	4
2012	3
2013	3
2014	3
2015	4
2016	6
2017	5
2018	1
2019	2
2020	2
2021	1
2022	4
2023	1
2024	0

1

Evidence for a common ethnic origin of cystic fibrosis mutation 3120+1G-->A in diverse populations.

Dörk T, El-Harith EH, Stuhrmann M, Macek M Jr, Egan M, Cutting GR, Tzetis M, Kanavakis E, Carles S, Claustres M, Padoa C, Ramsay M, Schmidtke J. Dörk T, et al. Am J Hum Genet. 1998 Aug;63(2):656-62. doi: 10.1086/301950. Am J Hum Genet. 1998. PMID: 9683582 Free PMC article. No abstract available.

2

Incidence of cystic fibrosis in five different states of Brazil as determined by screening of p.F508del, mutation at the CFTR gene in newborns and patients.

Raskin S, Pereira-Ferrari L, Reis FC, Abreu F, Marostica P, Rozov T, Cardieri J, Ludwig N, Valentin L, Rosario-Filho NA, Camargo Neto E, Lewis E, Giugliani R, Diniz EM, Culpi L, Phillip JA 3rd, Chakraborty R. Raskin S, et al. J Cyst Fibros. 2008 Jan;7(1):15-22. doi: 10.1016/j.jcf.2007.03.006. Epub 2007 Jun 4. J Cyst Fibros. 2008. PMID: 17544945 Free article.

3

CFTR structural rearrangements are not a major mutational mechanism in black and coloured southern African patients with cystic fibrosis.

De Carvalho CL, Ramsay M. De Carvalho CL, et al. S Afr Med J. 2009 Oct;99(10):724. S Afr Med J. 2009. PMID: 20128270 No abstract available.

4

Novel CFTR mutations in black cystic fibrosis patients.

Feuillet-Fieux MN, Ferrec M, Gigarel N, Thuillier L, Sermet I, Steffann J, Lenoir G, Bonnefont JP. Feuillet-Fieux MN, et al. Clin Genet. 2004 Apr;65(4):284-7. doi: 10.1111/j.1399-0004.2004.00230.x. Clin Genet. 2004. PMID: 15025720

5

Geographic distribution of cystic fibrosis transmembrane regulator gene mutations in Saudi Arabia.

Banjar H. Banjar H. East Mediterr Health J. 1999 Nov;5(6):1230-5. East Mediterr Health J. 1999. PMID: 11924117 Free article.

6

Identification of common cystic fibrosis mutations in African-Americans with cystic fibrosis increases the detection rate to 75%.

Macek M Jr, Mackova A, Hamosh A, Hilman BC, Selden RF, Lucotte G, Friedman KJ, Knowles MR, Rosenstein BJ, Cutting GR. Macek M Jr, et al. Am J Hum Genet. 1997 May;60(5):1122-7. Am J Hum Genet. 1997. PMID: 9150159 Free PMC article.

7

First report of CFTR mutations in black cystic fibrosis patients of southern African origin.

Carles S, Desgeorges M, Goldman A, Thiart R, Guittard C, Kitazos CA, de Ravel TJ, Westwood AT, Claustres M, Ramsay M. Carles S, et al. J Med Genet. 1996 Sep;33(9):802-4. doi: 10.1136/jmg.33.9.802. J Med Genet. 1996. PMID: 8880589 Free PMC article.

8

CFTR allelic heterogeneity in Brazil: historical and geographical perspectives and implications for screening and counseling for cystic fibrosis in this country.

Faucz FR, Souza DA, Olandoski M, Raskin S. Faucz FR, et al. J Hum Genet. 2010 Feb;55(2):71-6. doi: 10.1038/jhg.2009.123. Epub 2009 Nov 27. J Hum Genet. 2010. PMID: 19942933

9

Analysis of four diverse population groups indicates that a subset of cystic fibrosis mutations occur in common among Caucasians.

Cutting GR, Curristin SM, Nash E, Rosenstein BJ, Lerer I, Abeliovich D, Hill A, Graham C. Cutting GR, et al. Am J Hum Genet. 1992 Jun;50(6):1185-94. Am J Hum Genet. 1992. PMID: 1376017 Free PMC article.

10

WGA allows the molecular characterization of a novel large CFTR rearrangement in a black South African cystic fibrosis patient.

des Georges M, Guittard C, Templin C, Altiéri JP, de Carvalho C, Ramsay M, Claustres M. des Georges M, et al. J Mol Diagn. 2008 Nov;10(6):544-8. doi: 10.2353/jmoldx.2008.080028. Epub 2008 Oct 2. J Mol Diagn. 2008. PMID: 18832460 Free PMC article.

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