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Items: 1 to 20 of 114

1.

Frequency of common HFE variants in the Saudi population: a high throughput molecular beacon-based study.

Alsmadi OA, Al-Kayal F, Al-Hamed M, Meyer BF.

BMC Med Genet. 2006 May 3;7:43.

3.

Mutation analysis of the HFE gene in German hemochromatosis patients and controls using automated SSCP-based capillary electrophoresis and a new PCR-ELISA technique.

Hellerbrand C, Bosserhoff AK, Seegers S, Lingner G, Wrede C, Lock G, Schölmerich J, Büttner R.

Scand J Gastroenterol. 2001 Nov;36(11):1211-6.

PMID:
11686223
4.

Molecular diagnosis of hereditary hemochromatosis: application of a newly-developed reverse-hybridization assay in the South African population.

Kotze MJ, de Villiers JN, Bouwens CS, Warnich L, Zaahl MG, van der Merwe S, Oberkanins C.

Clin Genet. 2004 Apr;65(4):317-21.

PMID:
15025725
5.

[Molecular genetic diagnostics and screening of hereditary hemochromatosis].

Zlocha J, Kovács L, Pozgayová S, Kupcová V, Durínová S.

Vnitr Lek. 2006 Jun;52(6):602-8. Slovak.

PMID:
16871764
6.
7.

Validation of an unlabeled probe melting analysis assay combined with high-throughput extractions for genotyping of the most common variants in HFE-associated hereditary hemochromatosis, C282Y, H63D, and S65C.

Sumner K, Hubley L, Pont-Kingdon G, Mitchell S, Wayman T, Wilson A, Meadows C, Elenitoba-Johnson K, Pattison D, Dobrowolski S, Best H, Lyon E.

Genet Test Mol Biomarkers. 2012 Jul;16(7):656-60. doi: 10.1089/gtmb.2011.0204. Epub 2012 Feb 24.

PMID:
22364140
8.

Simultaneous detection of HFE C282Y, H63D and S65C mutations associated with type 1 haemochromatosis using a multiplex luminex bead assay.

Cardoso SP, Patel R, Brown C, Navarrete C.

Tissue Antigens. 2011 Sep;78(3):171-7. doi: 10.1111/j.1399-0039.2011.01736.x. Epub 2011 Jul 8.

PMID:
21736562
9.

Simultaneous detection of the C282Y, H63D and S65C mutations in the hemochromatosis gene using quenched-FRET real-time PCR.

Moysés CB, Moreira ES, Asprino PF, Guimarães GS, Alberto FL.

Braz J Med Biol Res. 2008 Oct;41(10):833-8.

10.

HFE mutations and hemochromatosis in Danish patients admitted for HFE genotyping.

Koefoed P, Dalhoff K, Dissing J, Kramer I, Milman N, Pedersen P, Simonsen K, Tygstrup N, Nielsen FC.

Scand J Clin Lab Invest. 2002;62(7):527-35.

PMID:
12512743
11.

Frequency of HFE H63D, S65C, and C282Y mutations in patients with iron overload and controls from Toledo, Spain.

de Diego C, Murga MJ, Martínez-Castro P.

Genet Test. 2004 Fall;8(3):263-7.

PMID:
15727249
12.

Mutations of the HFE gene among Turkish hereditary hemochromatosis patients.

Simsek H, Balaban YH, Yilmaz E, Sumer H, Buyukasik Y, Cengiz C, Ozcebe O, Hascelik G, Tatar G.

Ann Hematol. 2005 Oct;84(10):646-9. Epub 2005 May 4.

PMID:
15871018
13.

Genetic hemochromatosis, a Celtic disease: is it now time for population screening?

Byrnes V, Ryan E, Barrett S, Kenny P, Mayne P, Crowe J.

Genet Test. 2001 Summer;5(2):127-30.

PMID:
11551098
14.

Screening selected blood donors with biochemical iron overload for hemochromatosis: a regional experience.

De Gobbi M, D'Antico S, Castagno F, Testa D, Merlini R, Bondi A, Camaschella C.

Haematologica. 2004 Oct;89(10):1161-7.

15.

A 6-year survey of HFE gene test for hemochromatosis diagnosis.

Mura C, Raguénes O, Scotet V, Jacolot S, Mercier AY, Férec C.

Genet Med. 2005 Jan;7(1):68-73.

PMID:
15654232
16.

Prevalence of HFE mutations in California newborns.

Hoppe C, Watson RM, Long CM, Lorey F, Robles L, Klitz W, Styles L, Vichinsky E.

Pediatr Hematol Oncol. 2006 Sep;23(6):507-16.

PMID:
16849282
17.

Analysis of the HFE gene (C282Y, H63D and S65C) mutations in a general Chinese Han population.

Lin A, Yan WH, Xu HH, Zhu M, Zhou MY.

Tissue Antigens. 2007 Sep;70(3):252-5.

PMID:
17661915
18.

HFE gene mutations an Apulian population: allele frequencies.

Pietrapertosa A, Vitucci A, Campanale D, Palma A, Renni R, Delios G, Tannoia N.

Eur J Epidemiol. 2003;18(7):685-9.

PMID:
12952143
19.

Transferrin receptor-2 gene and non-C282Y homozygous patients with hemochromatosis.

Aguilar-Martinez P, Esculié-Coste C, Bismuth M, Giansily-Blaizot M, Larrey D, Schved JF.

Blood Cells Mol Dis. 2001 Jan-Feb;27(1):290-3.

PMID:
11358390
20.

Analysis of HFE and TFR2 mutations in selected blood donors with biochemical parameters of iron overload.

De Gobbi M, Daraio F, Oberkanins C, Moritz A, Kury F, Fiorelli G, Camaschella C.

Haematologica. 2003 Apr;88(4):396-401.

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