-
2
-
-
0029051968
-
Hemochromatosis screening in asymptomatic ambulatory men 30 years of age and older
-
Baer DM, Simons JL, Staples RL, Rumore GJ, Morton CJ. Hemochromatosis screening in asymptomatic ambulatory men 30 years of age and older. Am J Med 1995; 98:464-468.
-
(1995)
Am J Med
, vol.98
, pp. 464-468
-
-
Baer, D.M.1
Simons, J.L.2
Staples, R.L.3
Rumore, G.J.4
Morton, C.J.5
-
3
-
-
84867447690
-
H63D is an haemochromatosis associated allele: Reply
-
Powell LW, Goldwurm S. H63D is an haemochromatosis associated allele: reply. Gut 1998;43:442.
-
(1998)
Gut
, vol.43
, pp. 442
-
-
Powell, L.W.1
Goldwurm, S.2
-
4
-
-
9344224529
-
A novel MHC class I-like gene is mutation in patients with hereditary haemochromatosis
-
Feder JN, Gnirke A, Thomas W, et al. A novel MHC class I-like gene is mutation in patients with hereditary haemochromatosis. Nat Genet 1996;13:399-408.
-
(1996)
Nat Genet
, vol.13
, pp. 399-408
-
-
Feder, J.N.1
Gnirke, A.2
Thomas, W.3
-
5
-
-
0032496881
-
Hereditary hemochromatosis: Gene discovery and its implications for population-based screening
-
Burke W, Thomson E, Khoury M, et al. Hereditary hemochromatosis: gene discovery and its implications for population-based screening. JAMA 1998;280:172-178.
-
(1998)
JAMA
, vol.280
, pp. 172-178
-
-
Burke, W.1
Thomson, E.2
Khoury, M.3
-
6
-
-
0005600868
-
A simple genetic test identifies 90% of UK patients with haemochromatosis
-
The UK Haemochromatosis Consortium
-
The UK Haemochromatosis Consortium. A simple genetic test identifies 90% of UK patients with haemochromatosis. Gut 1997;41:841-844.
-
(1997)
Gut
, vol.41
, pp. 841-844
-
-
-
7
-
-
0007722114
-
H63D is an haemochromatosis associated allele
-
Fairbanks VF, Brandhagen DJ, Thiodeau SN, Snow K, Wollan PC. H63D is an haemochromatosis associated allele. Gut 1998;43:441.
-
(1998)
Gut
, vol.43
, pp. 441
-
-
Fairbanks, V.F.1
Brandhagen, D.J.2
Thiodeau, S.N.3
Snow, K.4
Wollan, P.C.5
-
9
-
-
0032914223
-
Simple multiplex PCR for the simultaneous detection of the C282Y and H63D hemochromatosis (HFE) gene mutations
-
Stott MK, Fellowes AP, Upton JD, Burt MJ, George PM. Simple multiplex PCR for the simultaneous detection of the C282Y and H63D hemochromatosis (HFE) gene mutations. Clin Chem 1999;45:426-428.
-
(1999)
Clin Chem
, vol.45
, pp. 426-428
-
-
Stott, M.K.1
Fellowes, A.P.2
Upton, J.D.3
Burt, M.J.4
George, P.M.5
-
10
-
-
0033016069
-
Genotyping single nucleotide polymorphisms by primer extension and high performance liquid chromatography
-
Hoogendoorn B, Owen MJ, Oefner PJ, Williams N, Austin J, O'Donovan MC. Genotyping single nucleotide polymorphisms by primer extension and high performance liquid chromatography. Hum Genet 1999;104: 89-93.
-
(1999)
Hum Genet
, vol.104
, pp. 89-93
-
-
Hoogendoorn, B.1
Owen, M.J.2
Oefner, P.J.3
Williams, N.4
Austin, J.5
O'Donovan, M.C.6
-
11
-
-
0030722621
-
Capillary electrophoresis for the detection of known point mutations by single-nucleotide primer extension and laserinduced fluorescence detection
-
Piggee CA, Muth J, Carrilho E, Karger BL. Capillary electrophoresis for the detection of known point mutations by single-nucleotide primer extension and laserinduced fluorescence detection. J Chromatogr A 1997; 781:367-375.
-
(1997)
J Chromatogr A
, vol.781
, pp. 367-375
-
-
Piggee, C.A.1
Muth, J.2
Carrilho, E.3
Karger, B.L.4
-
12
-
-
0343247681
-
Competitive oligonucleotide single-base extension combined with mass spectrometric detection for mutation screening
-
Higgins GS, Little DP, Köster H. Competitive oligonucleotide single-base extension combined with mass spectrometric detection for mutation screening. Biotechniques 1997;23:710-714.
-
(1997)
Biotechniques
, vol.23
, pp. 710-714
-
-
Higgins, G.S.1
Little, D.P.2
Köster, H.3
-
13
-
-
0031735108
-
Rapid detection of genetic mutations associated with haemochromatosis
-
Guttridge MG, Thompson J, Worwood M, Darke C. Rapid detection of genetic mutations associated with haemochromatosis. Vox Sang 1998;75:253-256.
-
(1998)
Vox Sang
, vol.75
, pp. 253-256
-
-
Guttridge, M.G.1
Thompson, J.2
Worwood, M.3
Darke, C.4
-
14
-
-
0030713023
-
A PCR-SSP method for detecting the Cys282Tyr mutation in the HFE gene associated with hereditary haemochromatosis
-
Smillie D. A PCR-SSP method for detecting the Cys282Tyr mutation in the HFE gene associated with hereditary haemochromatosis. Mol Pathol 1997;50:275-276.
-
(1997)
Mol Pathol
, vol.50
, pp. 275-276
-
-
Smillie, D.1
-
15
-
-
6844240223
-
Development of a multiplex ARMS test for mutations in the HFE gene associated with hereditary haemochromatosis
-
Baty D, Kwiatkowski AT, Mechan D, Harris A, Pippard MJ, Goudie D. Development of a multiplex ARMS test for mutations in the HFE gene associated with hereditary haemochromatosis. J Clin Pathol 1998;51:73-74.
-
(1998)
J Clin Pathol
, vol.51
, pp. 73-74
-
-
Baty, D.1
Kwiatkowski, A.T.2
Mechan, D.3
Harris, A.4
Pippard, M.J.5
Goudie, D.6
-
16
-
-
0030798387
-
Rapid genetic screening for haemochromatosis using heteroduplex technology
-
Jackson HA, Bowen DJ, Worwood M. Rapid genetic screening for haemochromatosis using heteroduplex technology. Br J Haematol 1997;98:856-859.
-
(1997)
Br J Haematol
, vol.98
, pp. 856-859
-
-
Jackson, H.A.1
Bowen, D.J.2
Worwood, M.3
-
17
-
-
0032973093
-
A rapid automated SSCP multiplex capillary electrophoresis protocol that detects the two common mutations implicated in hereditary hemochromatosis (HH)
-
Wenz HM, Baumhueter S, Ramachandra S, Worwood M. A rapid automated SSCP multiplex capillary electrophoresis protocol that detects the two common mutations implicated in hereditary hemochromatosis (HH). Hum Genet 1999;104:29-35.
-
(1999)
Hum Genet
, vol.104
, pp. 29-35
-
-
Wenz, H.M.1
Baumhueter, S.2
Ramachandra, S.3
Worwood, M.4
-
18
-
-
0028891143
-
Automated DNA purification and amplification from blood-stained cards using a robotic workstation
-
Belgrader P, Del Rio SA, Turner KA, Marino MA, Weaver KR, Williams PE. Automated DNA purification and amplification from blood-stained cards using a robotic workstation. Biotechniques 1995;19:426-432.
-
(1995)
Biotechniques
, vol.19
, pp. 426-432
-
-
Belgrader, P.1
Del Rio, S.A.2
Turner, K.A.3
Marino, M.A.4
Weaver, K.R.5
Williams, P.E.6
|