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Items: 1 to 20 of 161

1.

Detection of a cystic fibrosis modifier locus for meconium ileus on human chromosome 19q13.

Zielenski J, Corey M, Rozmahel R, Markiewicz D, Aznarez I, Casals T, Larriba S, Mercier B, Cutting GR, Krebsova A, Macek M Jr, Langfelder-Schwind E, Marshall BC, DeCelie-Germana J, Claustres M, Palacio A, Bal J, Nowakowska A, Ferec C, Estivill X, Durie P, Tsui LC.

Nat Genet. 1999 Jun;22(2):128-9. No abstract available.

PMID:
10369249
2.

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.

J Pediatr. 1989 May;114(5):767-73.

PMID:
2715890
3.

A CF modifier means meconium in mouse and man.

Whitcomb DC, Pogue-Geile KL.

Gastroenterology. 2000 Jul;119(1):268-9. No abstract available.

PMID:
10889182
4.

Genetic differences between cystic fibrosis with and without meconium ileus.

Mornet E, Simon-Bouy B, Serre JL, Estivill X, Farrall M, Williamson R, Boue J, Boue A.

Lancet. 1988 Feb 20;1(8582):376-8.

PMID:
2893188
5.

Familial occurrence of meconium ileus.

Allan JL, Robbie M, Phelan PD, Danks DM.

Eur J Pediatr. 1981 Feb;135(3):291-2.

PMID:
7227383
6.

Is meconium ileus genetically determined or associated with a more severe evolution of cystic fibrosis?

De Braekeleer M, Allard C, Leblanc JP, Aubin G, Simard F.

J Med Genet. 1998 Mar;35(3):262-3. No abstract available.

7.
8.

Genetic differences between cystic fibrosis with and without meconium ileus.

Curtis A, Jackson J, Keston M, Brock DJ.

Lancet. 1989 May 13;1(8646):1078-9. No abstract available.

PMID:
2566025
9.

Relative contribution of genetic and nongenetic modifiers to intestinal obstruction in cystic fibrosis.

Blackman SM, Deering-Brose R, McWilliams R, Naughton K, Coleman B, Lai T, Algire M, Beck S, Hoover-Fong J, Hamosh A, Fallin MD, West K, Arking DE, Chakravarti A, Cutler DJ, Cutting GR.

Gastroenterology. 2006 Oct;131(4):1030-9.

10.

Is the hemochromatosis gene a modifier locus for cystic fibrosis?

Rohlfs EM, Shaheen NJ, Silverman LM.

Genet Test. 1998;2(1):85-8.

PMID:
10464603
11.

ATB(0)/SLC1A5 gene. Fine localisation and exclusion of association with the intestinal phenotype of cystic fibrosis.

Larriba S, Sumoy L, Ramos MD, Giménez J, Estivill X, Casals T, Nunes V.

Eur J Hum Genet. 2001 Nov;9(11):860-6.

12.

Transmission ratio distortion and maternal effects confound the analysis of modulators of cystic fibrosis disease severity on 19q13.

Becker T, Jansen S, Tamm S, Wienker TF, Tümmler B, Stanke F.

Eur J Hum Genet. 2007 Jul;15(7):774-8.

13.

Hierarchical fine mapping of the cystic fibrosis modifier locus on 19q13 identifies an association with two elements near the genes CEACAM3 and CEACAM6.

Stanke F, Becker T, Hedtfeld S, Tamm S, Wienker TF, Tümmler B.

Hum Genet. 2010 Apr;127(4):383-94. doi: 10.1007/s00439-009-0779-6.

PMID:
20047061
14.

Modifier gene study of meconium ileus in cystic fibrosis: statistical considerations and gene mapping results.

Dorfman R, Li W, Sun L, Lin F, Wang Y, Sandford A, Paré PD, McKay K, Kayserova H, Piskackova T, Macek M, Czerska K, Sands D, Tiddens H, Margarit S, Repetto G, Sontag MK, Accurso FJ, Blackman S, Cutting GR, Tsui LC, Corey M, Durie P, Zielenski J, Strug LJ.

Hum Genet. 2009 Dec;126(6):763-78. doi: 10.1007/s00439-009-0724-8.

15.

Microsatellite markers for the cone-rod retinal dystrophy gene, CRX, on 19q13.3.

Bellingham J, Gregory-Evans CY, Gregory-Evans K.

J Med Genet. 1998 Jun;35(6):527. No abstract available.

16.

A candidate for the cystic fibrosis locus isolated by selection for methylation-free islands.

Estivill X, Farrall M, Scambler PJ, Bell GM, Hawley KM, Lench NJ, Bates GP, Kruyer HC, Frederick PA, Stanier P, et al.

Nature. 1987 Apr 30-May 6;326(6116):840-5.

PMID:
2883581
17.

Cystic fibrosis with and without meconium ileus.

Auvinet M, Morel Y, Chambon V, Andre J, Vidaud M, Goossens M, Bellon G, Gilly R.

Lancet. 1989 Jan 21;1(8630):161. No abstract available.

PMID:
2563077
18.

Genetic differences between cystic fibrosis with and without meconium ileus.

Simon-Bouy B, Serre JL, Mornet E, Tallandier A, Boué J, Boué A.

Lancet. 1989 Jul 8;2(8654):102. No abstract available.

PMID:
2567841
19.

A novel deletion in exon 12 (g1845delAG or g1846delGA) of the CFTR (ABCC7) gene in a CF infant presenting with meconium ileus.

Seia M, Cantù-Rajnoldi A, Ambrosioni A, Fiori S, Prandoni S, Corbetta C, Bassotti A, Moretti E, Giunta A, Padoan R.

Hum Mutat. 2000 Sep;16(3):279. No abstract available.

PMID:
10980555
20.

Failure of medical treatment in an adult cystic fibrosis patient with meconium ileus equivalent.

Khaitov S, Nissan A, Beglaibter N, Freund HR.

Tech Coloproctol. 2005 Apr;9(1):42-4.

PMID:
15868498

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