-
2
-
-
9344224529
-
A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis
-
Feder JN, Gnirke A, Thomas W, Tsuchihashi Z, et al. A novel MHC class I-like gene is mutated 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
Tsuchihashi, Z.4
-
5
-
-
0032697718
-
Hereditary hemochromatosis: Impact of molecular and iron-based testing on the diagnosis, treatment, and prevention of a common, chronic disease
-
Press RD. Hereditary hemochromatosis: Impact of molecular and iron-based testing on the diagnosis, treatment, and prevention of a common, chronic disease. Arch Pathol Lab Med 1999;123:1053-9.
-
(1999)
Arch Pathol Lab Med
, vol.123
, pp. 1053-1059
-
-
Press, R.D.1
-
6
-
-
0037708667
-
Guide to clinical preventive services
-
Baltimore: Williams Wilkins
-
Guide to clinical preventive services. In: US Preventive Services Task Force. 2nd ed. Baltimore: Williams Wilkins; 1996.
-
(1996)
US Preventive Services Task Force. 2nd ed.
-
-
-
7
-
-
0037151382
-
On the use of familial aggregation in population-based case probands for calculating penetrance
-
Begg CB. On the use of familial aggregation in population-based case probands for calculating penetrance. J Natl Cancer Inst 2002;94:1221-6.
-
(2002)
J Natl Cancer Inst
, vol.94
, pp. 1221-1226
-
-
Begg, C.B.1
-
8
-
-
0031957721
-
Heterogeneity of hemochromatosis in Italy
-
Piperno A, Sampietro M, Pietrangelo A, Arosio C, et al. Heterogeneity of hemochromatosis in Italy. Gastroenterology 1998;114:996-1002.
-
(1998)
Gastroenterology
, vol.114
, pp. 996-1002
-
-
Piperno, A.1
Sampietro, M.2
Pietrangelo, A.3
Arosio, C.4
-
9
-
-
0030294028
-
Haemochromatosis and HLA-H
-
[letter; comment]
-
Jazwinska EC, Cullen LM, Busfield F, Pyper W, et al. Haemochromatosis and HLA-H [letter; comment]. Nat Genet 1996;14:249-51.
-
(1996)
Nat Genet
, vol.14
, pp. 249-251
-
-
Jazwinska, E.C.1
Cullen, L.M.2
Busfield, F.3
Pyper, W.4
-
10
-
-
0031214025
-
A high prevalence of HLA-H 845A mutations in hemochromatosis patients and the normal population in eastern England
-
Willis G, Jennings BA, Goodman E, Fellows IW, Wimperis JZ. A high prevalence of HLA-H 845A mutations in hemochromatosis patients and the normal population in eastern England. Blood Cells Mol Dis 1997;23:288-91.
-
(1997)
Blood Cells Mol Dis
, vol.23
, pp. 288-291
-
-
Willis, G.1
Jennings, B.A.2
Goodman, E.3
Fellows, I.W.4
Wimperis, J.Z.5
-
11
-
-
0033764751
-
Contribution of different HFE genotypes to iron overload disease: A pooled analysis
-
Burke W, Imperatore G, McDonnell SM, Baron RC, Khoury MJ. Contribution of different HFE genotypes to iron overload disease: A pooled analysis. Genet Med 2000;2:271-7.
-
(2000)
Genet Med
, vol.2
, pp. 271-277
-
-
Burke, W.1
Imperatore, G.2
McDonnell, S.M.3
Baron, R.C.4
Khoury, M.J.5
-
12
-
-
0032851401
-
HFE genotypes and haemochromatosis: Quantifying the risk of disease
-
Lester S, Bardy P, McCluskey J. HFE genotypes and haemochromatosis: Quantifying the risk of disease. Tissue Antigens 1999;54:282-4.
-
(1999)
Tissue Antigens
, vol.54
, pp. 282-284
-
-
Lester, S.1
Bardy, P.2
McCluskey, J.3
-
13
-
-
0032401683
-
Hemochromatosis-associated mortality in the United States from 1979 to 1992: An analysis of Multiple-Cause Mortality Data
-
Yang Q, McDonnell SM, Khoury MJ, Cono J, Parrish RG. Hemochromatosis-associated mortality in the United States from 1979 to 1992: An analysis of Multiple-Cause Mortality Data. Ann Intern Med 1998;129:946-53.
-
(1998)
Ann Intern Med
, vol.129
, pp. 946-953
-
-
Yang, Q.1
McDonnell, S.M.2
Khoury, M.J.3
Cono, J.4
Parrish, R.G.5
-
14
-
-
0033517343
-
A population-based study of the clinical expression of the hemochromatosis gene
-
Olynyk JK, Cullen DJ, Aquilia S, Rossi E, Summerville L, Powell LW. A population-based study of the clinical expression of the hemochromatosis gene. N Engl J Med 1999;341:718-24.
-
(1999)
N Engl J Med
, vol.341
, pp. 718-724
-
-
Olynyk, J.K.1
Cullen, D.J.2
Aquilia, S.3
Rossi, E.4
Summerville, L.5
Powell, L.W.6
-
15
-
-
0017142698
-
Long term results of venesection therapy in idiopathic haemochromatosis
-
Bomford A, Williams R. Long term results of venesection therapy in idiopathic haemochromatosis. Q J Med 1976;45:611-23.
-
(1976)
Q J Med
, vol.45
, pp. 611-623
-
-
Bomford, A.1
Williams, R.2
-
16
-
-
0030340194
-
Population screening for haemochromatosis: A unifying analysis of published intervention trials
-
Bradley LA, Haddow JE, Palomaki GE. Population screening for haemochromatosis: A unifying analysis of published intervention trials. J Med Screen 1996;3:178-84.
-
(1996)
J Med Screen
, vol.3
, pp. 178-184
-
-
Bradley, L.A.1
Haddow, J.E.2
Palomaki, G.E.3
-
17
-
-
0034609577
-
The effect of HFE genotypes on measurements of iron overload in patients attending a health appraisal clinic
-
Beutler E, Felitti V, Gelbart T, Ho N. The effect of HFE genotypes on measurements of iron overload in patients attending a health appraisal clinic. Ann Intern Med 2000;133:329-37.
-
(2000)
Ann Intern Med
, vol.133
, pp. 329-337
-
-
Beutler, E.1
Felitti, V.2
Gelbart, T.3
Ho, N.4
-
18
-
-
0037132786
-
Penetrance of 845G→ A (C282Y) HFE hereditary haemochromatosis mutation in the USA
-
Beutler E, Felitti VJ, Koziol JA, Ho NJ, Gelbart T. Penetrance of 845G→ A (C282Y) HFE hereditary haemochromatosis mutation in the USA. Lancet 2002;359:211-8.
-
(2002)
Lancet
, vol.359
, pp. 211-218
-
-
Beutler, E.1
Felitti, V.J.2
Koziol, J.A.3
Ho, N.J.4
Gelbart, T.5
-
19
-
-
0030876559
-
Clinical features of genetic hemochromatosis in women compared with men
-
Moirand R, Adams PC, Bicheler V, Brissot P, Deugnier Y. Clinical features of genetic hemochromatosis in women compared with men. Ann Intern Med 1997;127:105-10.
-
(1997)
Ann Intern Med
, vol.127
, pp. 105-110
-
-
Moirand, R.1
Adams, P.C.2
Bicheler, V.3
Brissot, P.4
Deugnier, Y.5
-
20
-
-
0025146396
-
Factors affecting the concentrations of ferritin in serum in a healthy Australian population
-
Leggett BA, Brown NN, Bryant SJ, Duplock L, Powell LW, Halliday JW. Factors affecting the concentrations of ferritin in serum in a healthy Australian population. Clin Chem 1990;36:1350-5.
-
(1990)
Clin Chem
, vol.36
, pp. 1350-1355
-
-
Leggett, B.A.1
Brown, N.N.2
Bryant, S.J.3
Duplock, L.4
Powell, L.W.5
Halliday, J.W.6
-
21
-
-
0029963456
-
Iron in an Australian population: Too little or too much?
-
Leggett BA. Iron in an Australian population: Too little or too much? J Gastroenterol Hepatol 1996;11:1037-9.
-
(1996)
J Gastroenterol Hepatol
, vol.11
, pp. 1037-1039
-
-
Leggett, B.A.1
-
22
-
-
0033927849
-
Effects of HFE C282Y and H63D polymorphisms and polygenic background on iron stores in a large community sample of twins
-
Whitfield JB, Cullen LM, Jazwinska EC, Powell LW, et al. Effects of HFE C282Y and H63D polymorphisms and polygenic background on iron stores in a large community sample of twins. Am J Hum Genet 2000;66:1246-58.
-
(2000)
Am J Hum Genet
, vol.66
, pp. 1246-1258
-
-
Whitfield, J.B.1
Cullen, L.M.2
Jazwinska, E.C.3
Powell, L.W.4
-
23
-
-
0034572933
-
Iron homeostasis: Insights from genetics and animal models
-
Andrews NC. Iron homeostasis: Insights from genetics and animal models. Nat Rev Genet 2000;1:208-17.
-
(2000)
Nat Rev Genet
, vol.1
, pp. 208-217
-
-
Andrews, N.C.1
-
25
-
-
0033792885
-
Iron deficiency due to excessive therapeutic phlebotomy in hemochromatosis
-
Barton JC, Bottomley SS. Iron deficiency due to excessive therapeutic phlebotomy in hemochromatosis. Am J Hematol 2000;65:223-6.
-
(2000)
Am J Hematol
, vol.65
, pp. 223-226
-
-
Barton, J.C.1
Bottomley, S.S.2
-
26
-
-
0014447127
-
Venesection therapy in idiopathic haemochromatosis. An analysis of 40 treated and 18 untreated patients
-
Williams R, Smith PM, Spicer EJ, Barry M, Sherlock S. Venesection therapy in idiopathic haemochromatosis. An analysis of 40 treated and 18 untreated patients. Q J Med 1969;38:1-16.
-
(1969)
Q J Med
, vol.38
, pp. 1-16
-
-
Williams, R.1
Smith, P.M.2
Spicer, E.J.3
Barry, M.4
Sherlock, S.5
-
27
-
-
0029913626
-
Long-term survival in patients with hereditary hemochromatosis
-
Niederau C, Fischer R, Purschel A, Stremmel W, Haussinger D, Strohmeyer G. Long-term survival in patients with hereditary hemochromatosis. Gastroenterology 1996;110:1107-19.
-
(1996)
Gastroenterology
, vol.110
, pp. 1107-1119
-
-
Niederau, C.1
Fischer, R.2
Purschel, A.3
Stremmel, W.4
Haussinger, D.5
Strohmeyer, G.6
-
28
-
-
0025913745
-
Long-term survival analysis in hereditary hemochromatosis
-
Adams PC, Speechley M, Kertesz AE. Long-term survival analysis in hereditary hemochromatosis. Gastroenterology 1991;101:368-72.
-
(1991)
Gastroenterology
, vol.101
, pp. 368-372
-
-
Adams, P.C.1
Speechley, M.2
Kertesz, A.E.3
-
29
-
-
0033646187
-
DNA testing for haemochromatosis: Diagnostic, predictive and screening implications
-
Trent RJ, Le H, Yu B, Young G, Bowden DK. DNA testing for haemochromatosis: Diagnostic, predictive and screening implications. Pathology 2000;32:274-9.
-
(2000)
Pathology
, vol.32
, pp. 274-279
-
-
Trent, R.J.1
Le, H.2
Yu, B.3
Young, G.4
Bowden, D.K.5
-
30
-
-
0025115825
-
How serious are the adverse effects of screening?
-
Feldman W. How serious are the adverse effects of screening? J Gen Intern Med 1990;5:S50-3.
-
(1990)
J Gen Intern Med
, vol.5
-
-
Feldman, W.1
-
31
-
-
0034869504
-
Psychosocial impact of C282Y mutation testing for hemochromatosis
-
Power TE, Adams PC. Psychosocial impact of C282Y mutation testing for hemochromatosis. Genet Test 2001;5:107-10.
-
(2001)
Genet Test
, vol.5
, pp. 107-110
-
-
Power, T.E.1
Adams, P.C.2
-
32
-
-
0027937060
-
Genetic discrimination and screening for hemochromatosis
-
Alper JS, Geller LN, Barash CI, Billings PR, Laden V, Natowicz MR. Genetic discrimination and screening for hemochromatosis. J Public Health Policy 1994;15:345-58.
-
(1994)
J Public Health Policy
, vol.15
, pp. 345-358
-
-
Alper, J.S.1
Geller, L.N.2
Barash, C.I.3
Billings, P.R.4
Laden, V.5
Natowicz, M.R.6
-
33
-
-
0033855797
-
Genetic discrimination and screening for hemochromatosis: Then and now
-
Barash CI. Genetic discrimination and screening for hemochromatosis: Then and now. Genet Test 2000;4:213-8.
-
(2000)
Genet Test
, vol.4
, pp. 213-218
-
-
Barash, C.I.1
-
34
-
-
0037140203
-
Insurance agreement to facilitate genetic testing
-
Delatycki M, Allen K, Williamson R. Insurance agreement to facilitate genetic testing. Lancet 2002;359:1433.
-
(2002)
Lancet
, vol.359
, pp. 1433
-
-
Delatycki, M.1
Allen, K.2
Williamson, R.3
-
35
-
-
0030766989
-
Analysis of the cost of population screening for haemochromatosis using biochemical and genetic markers
-
Bassett ML, Leggett BA, Halliday JW, Webb S, Powell LW. Analysis of the cost of population screening for haemochromatosis using biochemical and genetic markers. J Hepatol 1997;27:517-24.
-
(1997)
J Hepatol
, vol.27
, pp. 517-524
-
-
Bassett, M.L.1
Leggett, B.A.2
Halliday, J.W.3
Webb, S.4
Powell, L.W.5
-
36
-
-
0032496881
-
Hereditary hemochromatosis: Gene discovery and its implications for population-based screening
-
Burke W, Thompson E, Khoury MJ, McDonnell DM, et al. Hereditary hemochromatosis: Gene discovery and its implications for population-based screening. J Am Med Assoc 1998;280:172-8.
-
(1998)
J Am Med Assoc
, vol.280
, pp. 172-178
-
-
Burke, W.1
Thompson, E.2
Khoury, M.J.3
McDonnell, D.M.4
-
37
-
-
0033848697
-
EASL International Consensus Conference on Haemochromatosis
-
Adams P, Brissot P, Powell LW. EASL International Consensus Conference on Haemochromatosis. J Hepatol 2000;33:485-504.
-
(2000)
J Hepatol
, vol.33
, pp. 485-504
-
-
Adams, P.1
Brissot, P.2
Powell, L.W.3
-
38
-
-
0030781497
-
Neonatal screening for the hemochromatosis defect
-
[Letter]
-
Cullen LM, Summerville L, Glassick TV, Grawford DH, Powell LW, Jazwinska EC. Neonatal screening for the hemochromatosis defect [Letter]. Blood 1997;90:4236-7.
-
(1997)
Blood
, vol.90
, pp. 4236-4237
-
-
Cullen, L.M.1
Summerville, L.2
Glassick, T.V.3
Grawford, D.H.4
Powell, L.W.5
Jazwinska, E.C.6
-
39
-
-
0031778690
-
The hemochromatosis 845 G→A and 187 C→G mutations: Prevalence in non-Caucasian populations
-
Cullen LM, Gao X, Easteal S, Jazwinska EC. The hemochromatosis 845 G→A and 187 C→G mutations: Prevalence in non-Caucasian populations. Am J Hum Genet 1998;62:1403-7
-
(1998)
Am J Hum Genet
, vol.62
, pp. 1403-1407
-
-
Cullen, L.M.1
Gao, X.2
Easteal, S.3
Jazwinska, E.C.4
-
40
-
-
0032988517
-
Genotyping as a diagnostic aid in genetic haemochromatosis
-
Rossi E, Henderson S, Chin CY, Olynyk J, et al. Genotyping as a diagnostic aid in genetic haemochromatosis. J Gastroenterol Hepatol 1999;14:427-30.
-
(1999)
J Gastroenterol Hepatol
, vol.14
, pp. 427-430
-
-
Rossi, E.1
Henderson, S.2
Chin, C.Y.3
Olynyk, J.4
-
41
-
-
0030865131
-
Efficient large-scale screening for the hemochromatosis susceptibility gene mutation
-
[letter]
-
Takeuchi T, Soejima H, Faed JM, Yun K. Efficient large-scale screening for the hemochromatosis susceptibility gene mutation [letter]. Blood 1997;90:2848-9.
-
(1997)
Blood
, vol.90
, pp. 2848-2849
-
-
Takeuchi, T.1
Soejima, H.2
Faed, J.M.3
Yun, K.4
-
42
-
-
0031793132
-
The significance of haemochromatosis gene mutations in the general population: Implications for screening
-
Burt MJ, George PM, Upton JD, Collett JA, et al. The significance of haemochromatosis gene mutations in the general population: Implications for screening. Gut 1998;43:830-6.
-
(1998)
Gut
, vol.43
, pp. 830-836
-
-
Burt, M.J.1
George, P.M.2
Upton, J.D.3
Collett, J.A.4
-
43
-
-
0032986271
-
High prevalence of the hemochromatosis-associated Cys282Tyr HFE gene mutation in a healthy Norwegian population in the city of Oslo, and its phenotypic expression
-
Distante S, Berg JP, Lande K, Haug E, Bell H. High prevalence of the hemochromatosis-associated Cys282Tyr HFE gene mutation in a healthy Norwegian population in the city of Oslo, and its phenotypic expression. Scand J Gastroenterol 1999;34:529-34.
-
(1999)
Scand J Gastroenterol
, vol.34
, pp. 529-534
-
-
Distante, S.1
Berg, J.P.2
Lande, K.3
Haug, E.4
Bell, H.5
-
44
-
-
0033866912
-
Population screening for hemochromatosis by PCR using sequence-specific primers
-
Guttridge MG, Carter K, Warwood M, Darke C. Population screening for hemochromatosis by PCR using sequence-specific primers. Genet Test 2000;4:111-4.
-
(2000)
Genet Test
, vol.4
, pp. 111-114
-
-
Guttridge, M.G.1
Carter, K.2
Warwood, M.3
Darke, C.4
-
45
-
-
0031839335
-
The effect of HFE mutations on serum ferritin and transferrin saturation in the Jersey population
-
Merryweather-Clarke AT, Worwood M, Parkinson L, Mattock C, et al. The effect of HFE mutations on serum ferritin and transferrin saturation in the Jersey population. Br J Haematol 1998;101:369-73.
-
(1998)
Br J Haematol
, vol.101
, pp. 369-373
-
-
Merryweather-Clarke, A.T.1
Worwood, M.2
Parkinson, L.3
Mattock, C.4
-
46
-
-
0033561342
-
HFE mutations analysis in 711 hemochromatosis probands: Evidence for S65C implication in mild form of hemochromatosis
-
Mura C, Raguenes O, Ferec C. HFE mutations analysis in 711 hemochromatosis probands: Evidence for S65C implication in mild form of hemochromatosis. Blood 1999;93:2502-5.
-
(1999)
Blood
, vol.93
, pp. 2502-2505
-
-
Mura, C.1
Raguenes, O.2
Ferec, C.3
-
47
-
-
0031744037
-
High incidence of the Cys 282 Tyr mutation in the HFE gene in the Irish population - Implications for haemochromatosis
-
Murphy S, Curran MD, McDougall N, Callendere ME, O'Brien CJ, Middleton D. High incidence of the Cys 282 Tyr mutation in the HFE gene in the Irish population - Implications for haemochromatosis. Tissue Antigens 1998;52:484-8.
-
(1998)
Tissue Antigens
, vol.52
, pp. 484-488
-
-
Murphy, S.1
Curran, M.D.2
McDougall, N.3
Callendere, M.E.4
O'Brien, C.J.5
Middleton, D.6
-
48
-
-
0032845794
-
Rapid and simple determination of hereditary haemochromatosis mutations by multiplex PCR-SSCP: Detection of a new polymorphic mutation
-
Simonsen K, Dissing J, Rudbeck L, Schwartz M. Rapid and simple determination of hereditary haemochromatosis mutations by multiplex PCR-SSCP: Detection of a new polymorphic mutation. Ann Hum Genet 1999;63:193-7.
-
(1999)
Ann Hum Genet
, vol.63
, pp. 193-197
-
-
Simonsen, K.1
Dissing, J.2
Rudbeck, L.3
Schwartz, M.4
-
49
-
-
0032826029
-
The influence of hemochromatosis mutations on iron overload of thalassemia major
-
Longo F, Zecchina G, Sbaiz L, Fischer R, Piga A, Camaschella C. The influence of hemochromatosis mutations on iron overload of thalassemia major. Haematologica 1999;84:799-803.
-
(1999)
Haematologica
, vol.84
, pp. 799-803
-
-
Longo, F.1
Zecchina, G.2
Sbaiz, L.3
Fischer, R.4
Piga, A.5
Camaschella, C.6
-
50
-
-
0033855628
-
A pilot C282Y hemochromatosis screening in Italian newborns by TaqMan technology
-
Restagno G, Gomez AM, Sbaiz L, De Gobbi M, et al. A pilot C282Y hemochromatosis screening in Italian newborns by TaqMan technology. Genet Test 2000;4:177-81.
-
(2000)
Genet Test
, vol.4
, pp. 177-181
-
-
Restagno, G.1
Gomez, A.M.2
Sbaiz, L.3
De Gobbi, M.4
-
51
-
-
0035064272
-
Frequency and biochemical expression of C282Y/H63D hemochromatosis (HFE) gene mutations in the healthy adult population in Italy
-
Cassaneli S, Pignatti E, Montosi G, Garuti C, et al. Frequency and biochemical expression of C282Y/H63D hemochromatosis (HFE) gene mutations in the healthy adult population in Italy. J Hepatol 2001;34:523-8.
-
(2001)
J Hepatol
, vol.34
, pp. 523-528
-
-
Cassanelli, S.1
Pignatti, E.2
Montosi, G.3
Garuti, C.4
-
52
-
-
0034919182
-
Analysis of haemochromatosis gene mutations in a population from the Mediterranean Basin
-
Campo S, Restuccia T, Villari D, Raffa G, et al. Analysis of haemochromatosis gene mutations in a population from the Mediterranean Basin. Liver 2001;21:233-6.
-
(2001)
Liver
, vol.21
, pp. 233-236
-
-
Campo, S.1
Restuccia, T.2
Villari, D.3
Raffa, G.4
-
53
-
-
17044442568
-
Prevalence of the Cys282Tyr and His63Asp HFE gene mutations in Spanish patients with hereditary hemochromatosis and in controls
-
Sanchez M, Bruguera M, Bosch J, Rodes J, Ballesta F, Oliva R. Prevalence of the Cys282Tyr and His63Asp HFE gene mutations in Spanish patients with hereditary hemochromatosis and in controls. J Hepatol 1998;29:725-8.
-
(1998)
J Hepatol
, vol.29
, pp. 725-728
-
-
Sanchez, M.1
Bruguera, M.2
Bosch, J.3
Rodes, J.4
Ballesta, F.5
Oliva, R.6
-
54
-
-
0035795607
-
Prevalence of C282Y and H63D mutations in the hemochromatosis (HFE) gene in the United States
-
Steinberg KK, Cogswell ME, Chang JC, Caudill SP, et al. Prevalence of C282Y and H63D mutations in the hemochromatosis (HFE) gene in the United States. J Am Med Assoc 2001;285:2216-22.
-
(2001)
J Am Med Assoc
, vol.285
, pp. 2216-2222
-
-
Steinberg, K.K.1
Cogswell, M.E.2
Chang, J.C.3
Caudill, S.P.4
-
55
-
-
0031777070
-
Hereditary haemochromatosis mutation frequencies in the general population
-
Bradley LA, Johnson DD, Palomaki GE, Haddow JE, Robertson NH, Ferrie RM. Hereditary haemochromatosis mutation frequencies in the general population. J Med Screen 1998;5:34-6.
-
(1998)
J Med Screen
, vol.5
, pp. 34-36
-
-
Bradley, L.A.1
Johnson, D.D.2
Palomaki, G.E.3
Haddow, J.E.4
Robertson, N.H.5
Ferrie, R.M.6
-
56
-
-
0033166882
-
Population-based screening for hemochromatosis using phenotypic and DNA testing among employees of health maintenance organizations in Springfield, Missouri
-
McDonnell SM, Hover A, Gloe D, Ou CY, Cogswell ME, Grummer-Strawn L. Population-based screening for hemochromatosis using phenotypic and DNA testing among employees of health maintenance organizations in Springfield, Missouri. Am J Med 1999;107:30-7.
-
(1999)
Am J Med
, vol.107
, pp. 30-37
-
-
McDonnell, S.M.1
Hover, A.2
Gloe, D.3
Ou, C.Y.4
Cogswell, M.E.5
Grummer-Strawn, L.6
-
57
-
-
0031132040
-
Rapid diagnosis of the HLA-H gene Cys 282 Tyr mutation in hemochromatosis by polymerase chain reaction - A very rare mutation in the Chinese population
-
[letter]
-
Chang JG, Liu TC, Lin SF. Rapid diagnosis of the HLA-H gene Cys 282 Tyr mutation in hemochromatosis by polymerase chain reaction - A very rare mutation in the Chinese population [letter]. Blood 1997;89:3492-3.
-
(1997)
Blood
, vol.89
, pp. 3492-3493
-
-
Chang, J.G.1
Liu, T.C.2
Lin, S.F.3
-
58
-
-
0034170208
-
HFE gene mutation, C282Y causing hereditary hemochromatosis in Caucasians is extremely rare in Korean population
-
Lee JY, Yoo KH, Hahn SH. HFE gene mutation, C282Y causing hereditary hemochromatosis in Caucasians is extremely rare in Korean population. J Korean Med Sci 2000;15:179-82.
-
(2000)
J Korean Med Sci
, vol.15
, pp. 179-182
-
-
Lee, J.Y.1
Yoo, K.H.2
Hahn, S.H.3
-
59
-
-
0032968375
-
Frequencies in the Japanese population of HFE gene mutations
-
Sohda T, Yanai J, Soejima H, Tamura K. Frequencies in the Japanese population of HFE gene mutations. Biochem Genet 1999;37:63-8.
-
(1999)
Biochem Genet
, vol.37
, pp. 63-68
-
-
Sohda, T.1
Yanai, J.2
Soejima, H.3
Tamura, K.4
-
60
-
-
0036177909
-
A population-based study of the biochemical and clinical expression of the H63D hemochromatosis mutation
-
Gochee PA, Powell LW, Cullen DJ, DuSart D, Rossi E, Olynyk JK. A population-based study of the biochemical and clinical expression of the H63D hemochromatosis mutation. Gastroenterol 2002;122:646-51.
-
(2002)
Gastroenterol
, vol.122
, pp. 646-651
-
-
Gochee, P.A.1
Powell, L.W.2
Cullen, D.J.3
DuSart, D.4
Rossi, E.5
Olynyk, J.K.6
|