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Items: 1 to 20 of 188

1.

Identification of the cystic fibrosis gene: genetic analysis.

Kerem B, Rommens JM, Buchanan JA, Markiewicz D, Cox TK, Chakravarti A, Buchwald M, Tsui LC.

Science. 1989 Sep 8;245(4922):1073-80.

PMID:
2570460
2.

DNA marker haplotype association with pancreatic sufficiency in cystic fibrosis.

Kerem BS, Buchanan JA, Durie P, Corey ML, Levison H, Rommens JM, Buchwald M, Tsui LC.

Am J Hum Genet. 1989 Jun;44(6):827-34.

3.
4.

[Relation between gene mutations and pancreatic exocrine function in patients with cystic fibrosis].

Radivojević D, Guć-Sćekić M, Djurisić M, Lalić T, Minić P, Kanavakis E.

Srp Arh Celok Lek. 2001 May-Jun;129 Suppl 1:6-9. Serbian.

PMID:
15637983
5.

Extended haplotype analysis of cystic fibrosis mutations and its implications for the selective advantage hypothesis.

Sereth H, Shoshani T, Bashan N, Kerem BS.

Hum Genet. 1993 Oct 1;92(3):289-95.

PMID:
7691712
6.

Cystic fibrosis: prenatal diagnosis and carrier detection by DNA analysis.

Nelson PV, Carey WF, Morris CP, Pollard AC.

Med J Aust. 1989 Aug 7;151(3):126-7, 130-1.

PMID:
2569156
7.
8.

Polymorphic DNA markers linked to cystic fibrosis locus in 20 Italian nuclear families.

Novelli G, Potenza L, Ruzzo A, Dallapiccola B.

Gene Geogr. 1987 Dec;1(3):193-9.

PMID:
3154126
9.
10.

Analysis of DNA probes for the prenatal diagnosis of cystic fibrosis.

Dry PJ, Wake S, Robertson CF, Colley P, Sheffield LJ.

Med J Aust. 1989 Aug 7;151(3):131, 133-6.

PMID:
2569157
11.

Direct gene diagnosis of cystic fibrosis by allele-specific polymerase chain reactions.

Wagner M, Schloesser M, Reiss J.

Mol Biol Med. 1990 Aug;7(4):359-64.

PMID:
1978221
12.

Patterns of polymorphism and linkage disequilibrium for cystic fibrosis.

Estivill X, Scambler PJ, Wainwright BJ, Hawley K, Frederick P, Schwartz M, Baiget M, Kere J, Williamson R, Farrall M.

Genomics. 1987 Nov;1(3):257-63.

PMID:
2895728
13.
14.

Mild cystic fibrosis linked to chromosome 7q22 markers with an uncommon haplotype.

McConkie-Rosell A, Chen YT, Harris D, Speer MC, Pericak-Vance MA, Ding JH, Highsmith WE Jr, Knowles M, Kahler SG.

Ann Intern Med. 1989 Nov 15;111(10):797-801.

PMID:
2817627
15.

Microsatellite haplotypes for cystic fibrosis: mutation frameworks and evolutionary tracers.

Morral N, Nunes V, Casals T, Chillón M, Giménez J, Bertranpetit J, Estivill X.

Hum Mol Genet. 1993 Jul;2(7):1015-22.

PMID:
7689896
16.

Three additional DNA polymorphisms in the met gene and D7S8 locus: use in prenatal diagnosis of cystic fibrosis.

Dean M, O'Connell P, Leppert M, Park M, Amos JA, Phillips DG, White R, Vande Woude GF.

J Pediatr. 1987 Oct;111(4):490-5.

PMID:
2888841
17.

CFTR haplotypic variability for normal and mutant genes in cystic fibrosis families from southern France.

Claustres M, Desgeorges M, Moine P, Morral N, Estivill X.

Hum Genet. 1996 Sep;98(3):336-44.

PMID:
8707306
18.

Cystic fibrosis: typing 89 German families with linked DNA probes.

Weber J, Aulehla-Scholz C, Kaiser R, Eigel A, Neugebauer M, Horst J, Olek K.

Hum Genet. 1988 Dec;81(1):54-6.

PMID:
2904405
19.

Risks of fetal cystic fibrosis based on linkage disequilibrium data.

Holloway S, Brock DJ.

Hum Genet. 1989 Aug;83(1):52-4.

PMID:
2570017
20.

Cystic fibrosis in a southern Brazilian population: characteristics of 90% of the alleles.

Faucz FR, Gimenez J, Ramos MD, Pereira-Ferrari L, Estivill X, Raskin S, Casals T, Culpi L.

Clin Genet. 2007 Sep;72(3):218-23.

PMID:
17718859
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