-
1
-
-
0036118773
-
Sideroblastic anemias
-
Alcindor T., and Bridges K.R. Sideroblastic anemias. Br J Hematol 116 4 (2002) 733-743
-
(2002)
Br J Hematol
, vol.116
, Issue.4
, pp. 733-743
-
-
Alcindor, T.1
Bridges, K.R.2
-
2
-
-
0001600748
-
Chronic refractory anemia with sideroblastic bone marrow: a study of four cases
-
Bjorkman S.E. Chronic refractory anemia with sideroblastic bone marrow: a study of four cases. Blood 11 (1956) 250-259
-
(1956)
Blood
, vol.11
, pp. 250-259
-
-
Bjorkman, S.E.1
-
3
-
-
0019952276
-
Proposals for the classification of the myelodysplastic syndromes
-
Bennett J.M., et al. Proposals for the classification of the myelodysplastic syndromes. Br J Hematol 51 2 (1982) 189-199
-
(1982)
Br J Hematol
, vol.51
, Issue.2
, pp. 189-199
-
-
Bennett, J.M.1
-
4
-
-
0036786901
-
The World Health Organization (WHO) classification of the myeloid neoplasms
-
Vardiman J.W., Harris N.L., and Brunning R.D. The World Health Organization (WHO) classification of the myeloid neoplasms. Blood 100 7 (2002) 2292-2302
-
(2002)
Blood
, vol.100
, Issue.7
, pp. 2292-2302
-
-
Vardiman, J.W.1
Harris, N.L.2
Brunning, R.D.3
-
5
-
-
0032004564
-
Diagnostic and biological significance of sideroblastic erythropoiesis in the myelodysplastic syndromes
-
Yoshida Y., et al. Diagnostic and biological significance of sideroblastic erythropoiesis in the myelodysplastic syndromes. Int J Hematol 67 2 (1998) 137-144
-
(1998)
Int J Hematol
, vol.67
, Issue.2
, pp. 137-144
-
-
Yoshida, Y.1
-
6
-
-
0020994491
-
Ring sideroblasts and myelodysplastic syndromes
-
Cazzola M. Ring sideroblasts and myelodysplastic syndromes. J Clin Pathol 36 12 (1983) 1413-1414
-
(1983)
J Clin Pathol
, vol.36
, Issue.12
, pp. 1413-1414
-
-
Cazzola, M.1
-
7
-
-
0026633427
-
Heterogeneity of acquired idiopathic sideroblastic anemia (AISA)
-
Garand R., et al. Heterogeneity of acquired idiopathic sideroblastic anemia (AISA). Leuk Res 16 5 (1992) 463-468
-
(1992)
Leuk Res
, vol.16
, Issue.5
, pp. 463-468
-
-
Garand, R.1
-
8
-
-
0025186898
-
Two types of acquired idiopathic sideroblastic anemia (AISA)
-
Gattermann N., Aul C., and Schneider W. Two types of acquired idiopathic sideroblastic anemia (AISA). Br J Hematol 74 1 (1990) 45-52
-
(1990)
Br J Hematol
, vol.74
, Issue.1
, pp. 45-52
-
-
Gattermann, N.1
Aul, C.2
Schneider, W.3
-
9
-
-
33748754872
-
Congenital sideroblastic anemias
-
Bottomley S.S. Congenital sideroblastic anemias. Curr Hematol Rep 5 1 (2006) 41-49
-
(2006)
Curr Hematol Rep
, vol.5
, Issue.1
, pp. 41-49
-
-
Bottomley, S.S.1
-
10
-
-
0036799489
-
The genetics of inherited sideroblastic anemias
-
Fleming M.D. The genetics of inherited sideroblastic anemias. Semin Hematol 39 4 (2002) 270-281
-
(2002)
Semin Hematol
, vol.39
, Issue.4
, pp. 270-281
-
-
Fleming, M.D.1
-
11
-
-
0028875262
-
Late-onset X-linked sideroblastic anemia. Missense mutations in the erythroid delta-aminolevulinate synthase (ALAS2) gene in two pyridoxine-responsive patients initially diagnosed with acquired refractory anemia and ringed sideroblasts [see comment]
-
Cotter P.D., et al. Late-onset X-linked sideroblastic anemia. Missense mutations in the erythroid delta-aminolevulinate synthase (ALAS2) gene in two pyridoxine-responsive patients initially diagnosed with acquired refractory anemia and ringed sideroblasts [see comment]. J Clin Invest 96 4 (1995) 2090-2096
-
(1995)
J Clin Invest
, vol.96
, Issue.4
, pp. 2090-2096
-
-
Cotter, P.D.1
-
12
-
-
0034672159
-
Familial-skewed X-chromosome inactivation as a predisposing factor for late-onset X-linked sideroblastic anemia in carrier females
-
Cazzola M., et al. Familial-skewed X-chromosome inactivation as a predisposing factor for late-onset X-linked sideroblastic anemia in carrier females. Blood 96 13 (2000) 4363-4365
-
(2000)
Blood
, vol.96
, Issue.13
, pp. 4363-4365
-
-
Cazzola, M.1
-
13
-
-
0032827236
-
A novel mutation of the erythroid-specific gamma-aminolevulinate synthase gene in a patient with non-inherited pyridoxine-responsive sideroblastic anemia
-
Harigae H., et al. A novel mutation of the erythroid-specific gamma-aminolevulinate synthase gene in a patient with non-inherited pyridoxine-responsive sideroblastic anemia. Am J Hematol 62 2 (1999) 112-114
-
(1999)
Am J Hematol
, vol.62
, Issue.2
, pp. 112-114
-
-
Harigae, H.1
-
14
-
-
6344220330
-
Onset of X-linked sideroblastic anemia in the fourth decade
-
Cortesao E., et al. Onset of X-linked sideroblastic anemia in the fourth decade. Hematologica 89 10 (2004) 1261-1263
-
(2004)
Hematologica
, vol.89
, Issue.10
, pp. 1261-1263
-
-
Cortesao, E.1
-
15
-
-
0037818369
-
A promoter mutation in the erythroid-specific 5-aminolevulinate synthase (ALAS2) gene causes X-linked sideroblastic anemia
-
Bekri S., et al. A promoter mutation in the erythroid-specific 5-aminolevulinate synthase (ALAS2) gene causes X-linked sideroblastic anemia. Blood 102 2 (2003) 698-704
-
(2003)
Blood
, vol.102
, Issue.2
, pp. 698-704
-
-
Bekri, S.1
-
16
-
-
0038819137
-
Late-onset X-linked sideroblastic anemia following hemodialysis
-
Furuyama K., et al. Late-onset X-linked sideroblastic anemia following hemodialysis. Blood 101 11 (2003) 4623-4624
-
(2003)
Blood
, vol.101
, Issue.11
, pp. 4623-4624
-
-
Furuyama, K.1
-
17
-
-
0033105568
-
Four new mutations in the erythroid-specific 5-aminolevulinate synthase (ALAS2) gene causing X-linked sideroblastic anemia: increased pyridoxine responsiveness after removal of iron overload by phlebotomy and coinheritance of hereditary hemochromatosis
-
Cotter P.D., et al. Four new mutations in the erythroid-specific 5-aminolevulinate synthase (ALAS2) gene causing X-linked sideroblastic anemia: increased pyridoxine responsiveness after removal of iron overload by phlebotomy and coinheritance of hereditary hemochromatosis. Blood 93 5 (1999) 1757-1769
-
(1999)
Blood
, vol.93
, Issue.5
, pp. 1757-1769
-
-
Cotter, P.D.1
-
18
-
-
0036483546
-
Multiple mechanisms for hereditary sideroblastic anemia
-
Furuyama K., and Sassa S. Multiple mechanisms for hereditary sideroblastic anemia. Cell Mol Biol (Noisy-le-grand) 48 1 (2002) 5-10
-
(2002)
Cell Mol Biol (Noisy-le-grand)
, vol.48
, Issue.1
, pp. 5-10
-
-
Furuyama, K.1
Sassa, S.2
-
19
-
-
11244252826
-
Acquired alpha-thalassemia in association with myelodysplastic syndrome and other hematologic malignancies
-
Steensma D.P., Gibbons R.J., and Higgs D.R. Acquired alpha-thalassemia in association with myelodysplastic syndrome and other hematologic malignancies. Blood 105 2 (2005) 443-452
-
(2005)
Blood
, vol.105
, Issue.2
, pp. 443-452
-
-
Steensma, D.P.1
Gibbons, R.J.2
Higgs, D.R.3
-
20
-
-
0026570135
-
The molecular defect of ferrochelatase in a patient with erythropoietic protoporphyria
-
Nakahashi Y., et al. The molecular defect of ferrochelatase in a patient with erythropoietic protoporphyria. Proc Natl Acad Sci USA 89 1 (1992) 281-285
-
(1992)
Proc Natl Acad Sci USA
, vol.89
, Issue.1
, pp. 281-285
-
-
Nakahashi, Y.1
-
21
-
-
0001025080
-
Erythropoietic protoporphyria. A new porphyria syndrome with solar urticaria due to protoporphyrinaemia
-
Magnus I.A., et al. Erythropoietic protoporphyria. A new porphyria syndrome with solar urticaria due to protoporphyrinaemia. Lancet 2 (1961) 448-451
-
(1961)
Lancet
, vol.2
, pp. 448-451
-
-
Magnus, I.A.1
-
22
-
-
0028149374
-
Erythropoietic protoporphyria
-
Todd D.J. Erythropoietic protoporphyria. Br J Dermatol 131 6 (1994) 751-766
-
(1994)
Br J Dermatol
, vol.131
, Issue.6
, pp. 751-766
-
-
Todd, D.J.1
-
23
-
-
0032128422
-
Molecular defects in ferrochelatase in patients with protoporphyria requiring liver transplantation
-
Bloomer J., et al. Molecular defects in ferrochelatase in patients with protoporphyria requiring liver transplantation. J Clin Invest 102 1 (1998) 107-114
-
(1998)
J Clin Invest
, vol.102
, Issue.1
, pp. 107-114
-
-
Bloomer, J.1
-
24
-
-
0027393011
-
Accumulation of iron in erythroblasts of patients with erythropoietic protoporphyria
-
Rademakers L.H., et al. Accumulation of iron in erythroblasts of patients with erythropoietic protoporphyria. Eur J Clin Invest 23 2 (1993) 130-138
-
(1993)
Eur J Clin Invest
, vol.23
, Issue.2
, pp. 130-138
-
-
Rademakers, L.H.1
-
25
-
-
0035675628
-
Late-onset erythropoietic porphyria caused by a chromosome 18q deletion in erythroid cells
-
Aplin C., et al. Late-onset erythropoietic porphyria caused by a chromosome 18q deletion in erythroid cells. J Invest Dermatol 117 6 (2001) 1647-1649
-
(2001)
J Invest Dermatol
, vol.117
, Issue.6
, pp. 1647-1649
-
-
Aplin, C.1
-
26
-
-
0030057636
-
Erythropoietic protoporphyria without cutaneous photosensitivity and with ringed sideroblasts in an atomic bomb survivor
-
Takeda Y., et al. Erythropoietic protoporphyria without cutaneous photosensitivity and with ringed sideroblasts in an atomic bomb survivor. Lancet 347 8998 (1996) 395-396
-
(1996)
Lancet
, vol.347
, Issue.8998
, pp. 395-396
-
-
Takeda, Y.1
-
27
-
-
0034219372
-
Myelodysplastic syndrome terminating in erythropoietic protoporphyria after 15 years of aplastic anemia
-
Shirota T., et al. Myelodysplastic syndrome terminating in erythropoietic protoporphyria after 15 years of aplastic anemia. Int J Hematol 72 1 (2000) 44-47
-
(2000)
Int J Hematol
, vol.72
, Issue.1
, pp. 44-47
-
-
Shirota, T.1
-
28
-
-
0026721373
-
Photosensitivity, abnormal porphyrin profile, and sideroblastic anemia
-
Lim H.W., et al. Photosensitivity, abnormal porphyrin profile, and sideroblastic anemia. J Am Acad Dermatol 27 2 Pt 2 (1992) 287-292
-
(1992)
J Am Acad Dermatol
, vol.27
, Issue.2 PART 2
, pp. 287-292
-
-
Lim, H.W.1
-
29
-
-
30144434692
-
Photosensitivity and acute liver injury in myeloproliferative disorder secondary to late-onset protoporphyria caused by deletion of a ferrochelatase gene in hematopoietic cells
-
Goodwin R.G., et al. Photosensitivity and acute liver injury in myeloproliferative disorder secondary to late-onset protoporphyria caused by deletion of a ferrochelatase gene in hematopoietic cells. Blood 107 1 (2006) 60-62
-
(2006)
Blood
, vol.107
, Issue.1
, pp. 60-62
-
-
Goodwin, R.G.1
-
30
-
-
0014673290
-
Sideroblastic anemia with dermal photosensitivity and greatly increased erythrocyte protoporphyrin
-
Rothstein G., Lee R., and Cartwright G.E. Sideroblastic anemia with dermal photosensitivity and greatly increased erythrocyte protoporphyrin. New Engl J Med 280 11 (1969) 587-590
-
(1969)
New Engl J Med
, vol.280
, Issue.11
, pp. 587-590
-
-
Rothstein, G.1
Lee, R.2
Cartwright, G.E.3
-
31
-
-
0029064443
-
Acquired hypochromic and microcytic sideroblastic anemia responsive to pyridoxine with low value of free erythrocyte protoporphyrin: a possible subgroup of idiopathic acquired sideroblastic anemia (IASA)
-
Takeda Y., et al. Acquired hypochromic and microcytic sideroblastic anemia responsive to pyridoxine with low value of free erythrocyte protoporphyrin: a possible subgroup of idiopathic acquired sideroblastic anemia (IASA). Br J Hematol 90 1 (1995) 207-209
-
(1995)
Br J Hematol
, vol.90
, Issue.1
, pp. 207-209
-
-
Takeda, Y.1
-
32
-
-
0013897485
-
The response of free erythrocyte protoporphyrin to pyridoxine therapy in a patient with sideroachrestic (sideroblastic) anemia
-
Lee G.R., Cartwright G.E., and Wintrobe M.M. The response of free erythrocyte protoporphyrin to pyridoxine therapy in a patient with sideroachrestic (sideroblastic) anemia. Blood 27 4 (1966) 557-567
-
(1966)
Blood
, vol.27
, Issue.4
, pp. 557-567
-
-
Lee, G.R.1
Cartwright, G.E.2
Wintrobe, M.M.3
-
33
-
-
0017332779
-
Porphyrin and iron metabolism in sideroblastic anemia
-
Bottomley S.S. Porphyrin and iron metabolism in sideroblastic anemia. Semin Hematol 14 2 (1977) 169-185
-
(1977)
Semin Hematol
, vol.14
, Issue.2
, pp. 169-185
-
-
Bottomley, S.S.1
-
34
-
-
0020062613
-
Sideroblastic anemia with markedly increased free erythrocyte protoporphyrin without dermal photosensitivity
-
Romslo I., et al. Sideroblastic anemia with markedly increased free erythrocyte protoporphyrin without dermal photosensitivity. Blood 59 3 (1982) 628-633
-
(1982)
Blood
, vol.59
, Issue.3
, pp. 628-633
-
-
Romslo, I.1
-
35
-
-
0019518106
-
Haem biosynthesis in refractory sideroblastic anemia associated with the preleukaemic syndrome
-
Pasanen A.V., et al. Haem biosynthesis in refractory sideroblastic anemia associated with the preleukaemic syndrome. Scand J Hematol 27 1 (1981) 35-44
-
(1981)
Scand J Hematol
, vol.27
, Issue.1
, pp. 35-44
-
-
Pasanen, A.V.1
-
37
-
-
0345404481
-
Rapid molecular diagnosis of erythropoietic protoporphyria among Swiss patients
-
Rufenacht U.B., et al. Rapid molecular diagnosis of erythropoietic protoporphyria among Swiss patients. Clin Chem Lab Med 36 10 (1998) 763-765
-
(1998)
Clin Chem Lab Med
, vol.36
, Issue.10
, pp. 763-765
-
-
Rufenacht, U.B.1
-
38
-
-
17844401454
-
A point mutation affecting an SP1 binding site in the promoter of the ferrochelatase gene impairs gene transcription and causes erythropoietic protoporphyria
-
Di Pierro E., et al. A point mutation affecting an SP1 binding site in the promoter of the ferrochelatase gene impairs gene transcription and causes erythropoietic protoporphyria. Exp Hematol 33 5 (2005) 584-591
-
(2005)
Exp Hematol
, vol.33
, Issue.5
, pp. 584-591
-
-
Di Pierro, E.1
-
39
-
-
0031717103
-
Mutations in the ferrochelatase gene of four Spanish patients with erythropoietic protoporphyria
-
Gouya L., et al. Mutations in the ferrochelatase gene of four Spanish patients with erythropoietic protoporphyria. J Invest Dermatol 111 3 (1998) 406-409
-
(1998)
J Invest Dermatol
, vol.111
, Issue.3
, pp. 406-409
-
-
Gouya, L.1
-
40
-
-
0036481404
-
Ferrochelatase gene mutations in erythropoietic protoporphyria: focus on liver disease
-
Chen F.P., et al. Ferrochelatase gene mutations in erythropoietic protoporphyria: focus on liver disease. Cell Mol Biol (Noisy-le-grand) 48 1 (2002) 83-89
-
(2002)
Cell Mol Biol (Noisy-le-grand)
, vol.48
, Issue.1
, pp. 83-89
-
-
Chen, F.P.1
-
41
-
-
1542283736
-
Acquired somatic ATRX mutations in myelodysplastic syndrome associated with alpha thalassemia (ATMDS) convey a more severe hematologic phenotype than germline ATRX mutations
-
Steensma D.P., et al. Acquired somatic ATRX mutations in myelodysplastic syndrome associated with alpha thalassemia (ATMDS) convey a more severe hematologic phenotype than germline ATRX mutations. Blood 103 6 (2004) 2019-2026
-
(2004)
Blood
, vol.103
, Issue.6
, pp. 2019-2026
-
-
Steensma, D.P.1
-
42
-
-
0037298128
-
The myelodysplastic syndrome(s): a perspective and review highlighting current controversies
-
Steensma D.P., and Tefferi A. The myelodysplastic syndrome(s): a perspective and review highlighting current controversies. Leuk Res 27 2 (2003) 95-120
-
(2003)
Leuk Res
, vol.27
, Issue.2
, pp. 95-120
-
-
Steensma, D.P.1
Tefferi, A.2
-
43
-
-
17344392308
-
A new mathematical model for relative quantification in real-time RT-PCR
-
Pfaffl M.W. A new mathematical model for relative quantification in real-time RT-PCR. Nucleic Acids Res 29 9 (2001) e45
-
(2001)
Nucleic Acids Res
, vol.29
, Issue.9
-
-
Pfaffl, M.W.1
-
44
-
-
13344292705
-
Quantitation of erythrocyte protoporphyrins and zinc protoporphyrin by high-pressure liquid chromatography
-
Ford R.E., and Ellefson R.D. Quantitation of erythrocyte protoporphyrins and zinc protoporphyrin by high-pressure liquid chromatography. Clin Chem 30 (1984) 972
-
(1984)
Clin Chem
, vol.30
, pp. 972
-
-
Ford, R.E.1
Ellefson, R.D.2
-
45
-
-
0036337671
-
The penetrance of dominant erythropoietic protoporphyria is modulated by expression of wildtype FECH
-
Gouya L., et al. The penetrance of dominant erythropoietic protoporphyria is modulated by expression of wildtype FECH. Nat Genet 30 1 (2002) 27-28
-
(2002)
Nat Genet
, vol.30
, Issue.1
, pp. 27-28
-
-
Gouya, L.1
-
46
-
-
0142058045
-
Genotypic determinants of phenotype in North American patients with erythropoietic protoporphyria
-
Risheg H., Chen F.P., and Bloomer J.R. Genotypic determinants of phenotype in North American patients with erythropoietic protoporphyria. Mol Genet Metab 80 1-2 (2003) 196-206
-
(2003)
Mol Genet Metab
, vol.80
, Issue.1-2
, pp. 196-206
-
-
Risheg, H.1
Chen, F.P.2
Bloomer, J.R.3
-
47
-
-
16544379257
-
Autosomal recessive erythropoietic protoporphyria in the United Kingdom: prevalence and relationship to liver disease
-
Whatley S.D., et al. Autosomal recessive erythropoietic protoporphyria in the United Kingdom: prevalence and relationship to liver disease. J Med Genet 41 8 (2004) e105
-
(2004)
J Med Genet
, vol.41
, Issue.8
-
-
Whatley, S.D.1
-
48
-
-
33745615399
-
Gene expression profiles of CD34+ cells in myelodysplastic syndromes: involvement of interferon stimulated genes and correlation to FAB subtype and karyotype
-
Pellagatti A., et al. Gene expression profiles of CD34+ cells in myelodysplastic syndromes: involvement of interferon stimulated genes and correlation to FAB subtype and karyotype. Blood (2006)
-
(2006)
Blood
-
-
Pellagatti, A.1
-
49
-
-
0038281403
-
Mitochondrial DNA mutations in patients with myelodysplastic syndromes
-
Shin M.G., et al. Mitochondrial DNA mutations in patients with myelodysplastic syndromes. Blood 101 8 (2003) 3118-3125
-
(2003)
Blood
, vol.101
, Issue.8
, pp. 3118-3125
-
-
Shin, M.G.1
-
50
-
-
0027753864
-
Is acquired idiopathic sideroblastic anemia (AISA) a disorder of mitochondrial DNA?
-
Gattermann N., Aul C., and Schneider W. Is acquired idiopathic sideroblastic anemia (AISA) a disorder of mitochondrial DNA?. Leukemia 7 12 (1993) 2069-2076
-
(1993)
Leukemia
, vol.7
, Issue.12
, pp. 2069-2076
-
-
Gattermann, N.1
Aul, C.2
Schneider, W.3
-
51
-
-
84885540938
-
Abstract 3542: acquired sideroblastic anemia unresponsive to pyridoxine caused by a somatic mutation in ALA synthase 2
-
May A., Al-Sabah A.I., and Lawless S.L. Abstract 3542: acquired sideroblastic anemia unresponsive to pyridoxine caused by a somatic mutation in ALA synthase 2. Blood 106 11 (2005)
-
(2005)
Blood
, vol.106
, Issue.11
-
-
May, A.1
Al-Sabah, A.I.2
Lawless, S.L.3
-
52
-
-
0037372442
-
Mitochondrial ferritin expression in erythroid cells from patients with sideroblastic anemia
-
Cazzola M., et al. Mitochondrial ferritin expression in erythroid cells from patients with sideroblastic anemia. Blood 101 5 (2003) 1996-2000
-
(2003)
Blood
, vol.101
, Issue.5
, pp. 1996-2000
-
-
Cazzola, M.1
-
53
-
-
22044434111
-
Aberrant mitochondrial iron distribution and maturation arrest characterize early erythroid precursors in low-risk myelodysplastic syndromes
-
Tehranchi R., et al. Aberrant mitochondrial iron distribution and maturation arrest characterize early erythroid precursors in low-risk myelodysplastic syndromes. Blood 106 1 (2005) 247-253
-
(2005)
Blood
, vol.106
, Issue.1
, pp. 247-253
-
-
Tehranchi, R.1
-
54
-
-
0034494799
-
Increased apoptosis in acquired sideroblastic anemia
-
Matthes T.W., et al. Increased apoptosis in acquired sideroblastic anemia. Br J Hematol 111 3 (2000) 843-852
-
(2000)
Br J Hematol
, vol.111
, Issue.3
, pp. 843-852
-
-
Matthes, T.W.1
-
55
-
-
2942563736
-
Gene expression profiling in the myelodysplastic syndromes using cDNA microarray technology
-
Pellagatti A., et al. Gene expression profiling in the myelodysplastic syndromes using cDNA microarray technology. Br J Hematol 125 5 (2004) 576-583
-
(2004)
Br J Hematol
, vol.125
, Issue.5
, pp. 576-583
-
-
Pellagatti, A.1
-
56
-
-
0030725676
-
Erythropoietic protoporphyria: four novel frameshift mutations in the ferrochelatase gene
-
Wang X., et al. Erythropoietic protoporphyria: four novel frameshift mutations in the ferrochelatase gene. J Invest Dermatol 109 5 (1997) 688-691
-
(1997)
J Invest Dermatol
, vol.109
, Issue.5
, pp. 688-691
-
-
Wang, X.1
-
57
-
-
0027204088
-
Identification of a single base pair deletion (40 del G) in exon 1 of the ferrochelatase gene in patients with erythropoietic protoporphyria
-
Todd D.J., et al. Identification of a single base pair deletion (40 del G) in exon 1 of the ferrochelatase gene in patients with erythropoietic protoporphyria. Hum Mol Genet 2 9 (1993) 1495-1496
-
(1993)
Hum Mol Genet
, vol.2
, Issue.9
, pp. 1495-1496
-
-
Todd, D.J.1
-
58
-
-
0034908554
-
Nomenclature for the description of human sequence variations
-
den Dunnen J.T., and Antonarakis S.E. Nomenclature for the description of human sequence variations. Hum Genet 109 1 (2001) 121-124
-
(2001)
Hum Genet
, vol.109
, Issue.1
, pp. 121-124
-
-
den Dunnen, J.T.1
Antonarakis, S.E.2
|