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Similar articles for PubMed (Select 2570460)

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.

XV-2c and KM.19 haplotype analysis in Chilean patients with cystic fibrosis and unknown CFTR gene mutations.

Repetto GM, Puga AR, Delgado I.

Biol Res. 2007;40(2):223-9. Epub 2007 Nov 21.

8.

Benign missense variations in the cystic fibrosis gene.

Kobayashi K, Knowles MR, Boucher RC, O'Brien WE, Beaudet AL.

Am J Hum Genet. 1990 Oct;47(4):611-5.

9.

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
10.
11.

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
12.

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
13.

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
14.
15.

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
16.

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
17.

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
18.

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
19.

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
20.

Risks of fetal cystic fibrosis based on linkage disequilibrium data.

Holloway S, Brock DJ.

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

PMID:
2570017
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