-
1
-
-
0026536404
-
The meiotic stage of nondisjunction in trisomy 21: Determination by using DNA polymorphisms
-
Antonarakis SE, Petersen MB, McInnis MG, Adelsberger PA, Schinzel AA, Binkert F, Pangalos C, Raoul O, Slaugenhaupt SA, Hafez M (1992) The meiotic stage of nondisjunction in trisomy 21: determination by using DNA polymorphisms. Am J Hum Genet 50:544-550
-
(1992)
Am J Hum Genet
, vol.50
, pp. 544-550
-
-
Antonarakis, S.E.1
Petersen, M.B.2
McInnis, M.G.3
Adelsberger, P.A.4
Schinzel, A.A.5
Binkert, F.6
Pangalos, C.7
Raoul, O.8
Slaugenhaupt, S.A.9
Hafez, M.10
-
2
-
-
31544435459
-
Methylenetetrahydrofolate reductase gene polymorphisms and their association with trisomy 21
-
Acacio GL, Barini R, Bertuzzo CS, Couto EC, Annichino-Bizzacchi JM, Junior WP (2005) Methylenetetrahydrofolate reductase gene polymorphisms and their association with trisomy 21. Prenat Diagn 25:1196-1199
-
(2005)
Prenat Diagn
, vol.25
, pp. 1196-1199
-
-
Acacio, G.L.1
Barini, R.2
Bertuzzo, C.S.3
Couto, E.C.4
Annichino-Bizzacchi, J.M.5
Junior, W.P.6
-
3
-
-
0028659004
-
Operating characteristics of a rank correlation test for publication bias
-
Begg CB, Mazumdar M (1994) Operating characteristics of a rank correlation test for publication bias. Biometrics 50:1088-1101
-
(1994)
Biometrics
, vol.50
, pp. 1088-1101
-
-
Begg, C.B.1
Mazumdar, M.2
-
4
-
-
0030979178
-
Folate deficiency causes uracil misincorporation into human DNA and chromosome breakage: Implications for cancer and neuronal damage
-
Blount BC, Mack MM, Wehr CM, MacGregor JT, Hiatt RA, Wang G, Wickramasinghe SN, Everson RB, Ames BN (1997) Folate deficiency causes uracil misincorporation into human DNA and chromosome breakage: implications for cancer and neuronal damage. Proc Natl Acad Sci USA 7:3290-3295
-
(1997)
Proc Natl Acad Sci USA
, vol.7
, pp. 3290-3295
-
-
Blount, B.C.1
MacK, M.M.2
Wehr, C.M.3
MacGregor, J.T.4
Hiatt, R.A.5
Wang, G.6
Wickramasinghe, S.N.7
Everson, R.B.8
Ames, B.N.9
-
5
-
-
3142777011
-
Methylenetetrahydrofolate reductase enzyme polymorphisms as maternal risk for Down syndrome among Turkish women
-
Boduroglu K, Alanay Y, Koldan B, Tuncbilek E (2004) Methylenetetrahydrofolate reductase enzyme polymorphisms as maternal risk for Down syndrome among Turkish women. Am J Med Genet A 127:5-10
-
(2004)
Am J Med Genet a
, vol.127
, pp. 5-10
-
-
Boduroglu, K.1
Alanay, Y.2
Koldan, B.3
Tuncbilek, E.4
-
6
-
-
25444482825
-
No association between common polymorphisms in genes of folate and homocysteine metabolism and the risk of Down's syndrome among French mothers
-
Chango A, Fillon-Emery N, Mircher C, Blehaut H, Lambert D, Herbeth B, James SJ, Rethore MO, Nicolas JP (2005) No association between common polymorphisms in genes of folate and homocysteine metabolism and the risk of Down's syndrome among French mothers. Br J Nutr 94:166-169
-
(2005)
Br J Nutr
, vol.94
, pp. 166-169
-
-
Chango, A.1
Fillon-Emery, N.2
Mircher, C.3
Blehaut, H.4
Lambert, D.5
Herbeth, B.6
James, S.J.7
Rethore, M.O.8
Nicolas, J.P.9
-
7
-
-
0035922669
-
Epidemiological methods for studying genes and environmental factors in complex diseases
-
Clayton D, McKeigue PM (2001) Epidemiological methods for studying genes and environmental factors in complex diseases. Lancet 358:1356-1360
-
(2001)
Lancet
, vol.358
, pp. 1356-1360
-
-
Clayton, D.1
McKeigue, P.M.2
-
8
-
-
41049093347
-
The combination of estimates from different experiments
-
Cochran WG (1954) The combination of estimates from different experiments. Biometrics 10:101-129
-
(1954)
Biometrics
, vol.10
, pp. 101-129
-
-
Cochran, W.G.1
-
9
-
-
85026168559
-
What we do and don't know about 'race', 'ethnicity', genetics and health at the dawn of the genome era
-
Collins FS (2004) What we do and don't know about 'race', 'ethnicity', genetics and health at the dawn of the genome era. Nat Genet 36:S13-S15
-
(2004)
Nat Genet
, vol.36
-
-
Collins, F.S.1
-
10
-
-
33646240576
-
Folate gene polymorphisms and the risk of Down syndrome pregnancies in young Italian women
-
Coppede F, Marini G, Bargagna S, Stuppia L, Minichilli F, Fontana I, Colognato R, Astrea G, Palka G, Migliore L (2006) Folate gene polymorphisms and the risk of Down syndrome pregnancies in young Italian women. Am J Med Genet A 140:1083-1091
-
(2006)
Am J Med Genet a
, vol.140
, pp. 1083-1091
-
-
Coppede, F.1
Marini, G.2
Bargagna, S.3
Stuppia, L.4
Minichilli, F.5
Fontana, I.6
Colognato, R.7
Astrea, G.8
Palka, G.9
Migliore, L.10
-
11
-
-
19944404258
-
Relationship between polymorphisms in genes involved in homocysteine metabolism and maternal risk for Down syndrome in Brazil
-
da Silva LR, Vergani N, Galdieri Lde C, Ribeiro Porto MP, Longhitano SB, Brunoni D, D'Almeida V, Alvarez Perez AB (2005) Relationship between polymorphisms in genes involved in homocysteine metabolism and maternal risk for Down syndrome in Brazil. Am J Med Genet A 135:263-267
-
(2005)
Am J Med Genet a
, vol.135
, pp. 263-267
-
-
Da Silva, L.R.1
Vergani, N.2
Galdieri Lde, C.3
Ribeiro Porto, M.P.4
Longhitano, S.B.5
Brunoni, D.6
D'Almeida, V.7
Alvarez Perez, A.B.8
-
12
-
-
0029049553
-
A candidate genetic risk factor for vascular disease: A common mutation in methylenetetrahydrofolate reductase
-
Frosst P, Blom HJ, Milos R, Goyette P, Sheppard CA, Matthews RG, Boers GJ, den Heijer M, Kluijtmans LA, van den Heuvel LP (1995) A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase. Nat Genet 10:111-113
-
(1995)
Nat Genet
, vol.10
, pp. 111-113
-
-
Frosst, P.1
Blom, H.J.2
Milos, R.3
Goyette, P.4
Sheppard, C.A.5
Matthews, R.G.6
Boers, G.J.7
Den Heijer, M.8
Kluijtmans, L.A.9
Van Den Heuvel, L.P.10
-
14
-
-
0035459399
-
The power of statistical tests in meta-analysis
-
Hedges LV, Pigott DP (2001) The power of statistical tests in meta-analysis. Psychol Methods 6:203-217
-
(2001)
Psychol Methods
, vol.6
, pp. 203-217
-
-
Hedges, L.V.1
Pigott, D.P.2
-
15
-
-
0033846999
-
Polymorphisms in genes involved in folate metabolism as maternal risk factors for Down syndrome
-
Hobbs CA, Sherman SL, Yi P, Hopkins SE, Torfs CP, Hine RJ, Pogribna M, Rozen R, James SJ (2000) Polymorphisms in genes involved in folate metabolism as maternal risk factors for Down syndrome. Am J Hum Genet 67:623-630
-
(2000)
Am J Hum Genet
, vol.67
, pp. 623-630
-
-
Hobbs, C.A.1
Sherman, S.L.2
Yi, P.3
Hopkins, S.E.4
Torfs, C.P.5
Hine, R.J.6
Pogribna, M.7
Rozen, R.8
James, S.J.9
-
16
-
-
0037111008
-
Preferential transmission of the MTHFR 677 T allele to infants with Down syndrome: Implications for a survival advantage
-
Hobbs CA, Cleves MA, Lauer RM, Burns TL, James SJ (2002) Preferential transmission of the MTHFR 677 T allele to infants with Down syndrome: implications for a survival advantage. Am J Med Genet 113:9-14
-
(2002)
Am J Med Genet
, vol.113
, pp. 9-14
-
-
Hobbs, C.A.1
Cleves, M.A.2
Lauer, R.M.3
Burns, T.L.4
James, S.J.5
-
17
-
-
33846563409
-
Why most published research findings are false
-
Ioannidis JPA (2005) Why most published research findings are false. PLoS Med 2:e124
-
(2005)
PLoS Med
, vol.2
, pp. 124
-
-
Ioannidis, J.P.A.1
-
18
-
-
9644263985
-
'Racial' differences in genetic effects for complex diseases
-
Ioannidis JP, Ntzani EE, Trikalinos TA (2004) 'Racial' differences in genetic effects for complex diseases. Nat Genet 36:1312-1318
-
(2004)
Nat Genet
, vol.36
, pp. 1312-1318
-
-
Ioannidis, J.P.1
Ntzani, E.E.2
Trikalinos, T.A.3
-
19
-
-
3142737186
-
Maternal metabolic phenotype and risk of Down syndrome: Beyond genetics
-
James SJ (2004) Maternal metabolic phenotype and risk of Down syndrome: beyond genetics. Am J Med Genet A 127:1-4
-
(2004)
Am J Med Genet a
, vol.127
, pp. 1-4
-
-
James, S.J.1
-
20
-
-
0032845227
-
Abnormal folate metabolism and mutation in the methylenetetrahydrofolate reductase gene may be maternal risk factors for Down syndrome.
-
James SJ, Pogribna M, Pogribny IP, Melnyk S, Hine RJ, Gibson JB, Yi P, Tafoya DL, Swenson DH, Wilson VL, Gaylor DW (1999) Abnormal folate metabolism and mutation in the methylenetetrahydrofolate reductase gene may be maternal risk factors for Down syndrome. Am J Clin Nutr 70:495-501
-
(1999)
Am J Clin Nutr
, vol.70
, pp. 495-501
-
-
James, S.J.1
Pogribna, M.2
Pogribny, I.P.3
Melnyk, S.4
Hine, R.J.5
Gibson, J.B.6
Yi, P.7
Tafoya, D.L.8
Swenson, D.H.9
Wilson, V.L.10
Gaylor, D.W.11
-
21
-
-
85031896203
-
Genetic variation, classification and 'race'
-
Jorde LB, Wooding SP (2004) Genetic variation, classification and 'race'. Nat Genet 36:S28-S33
-
(2004)
Nat Genet
, vol.36
-
-
Jorde, L.B.1
Wooding, S.P.2
-
22
-
-
34548308987
-
Genetic variation associated with ischemic heart failure: A HuGE review and meta-analysis
-
Kitsios G, Zintzaras E (2007) Genetic variation associated with ischemic heart failure: a HuGE review and meta-analysis. Am J Epidemiol 166(6):619-633
-
(2007)
Am J Epidemiol
, vol.166
, Issue.6
, pp. 619-633
-
-
Kitsios, G.1
Zintzaras, E.2
-
23
-
-
0026652019
-
Cumulative meta-analysis of therapeutic trials for myocardial infarction
-
Lau J, Antman EM, Jimenez-Silva J, Kupelnick B, Mosteller F, Chalmers TC (1992) Cumulative meta-analysis of therapeutic trials for myocardial infarction. N Engl J Med 327:248-254
-
(1992)
N Engl J Med
, vol.327
, pp. 248-254
-
-
Lau, J.1
Antman, E.M.2
Jimenez-Silva, J.3
Kupelnick, B.4
Mosteller, F.5
Chalmers, T.C.6
-
24
-
-
0032501730
-
Summing up evidence: One answer is not always enough
-
Lau J, Ioannidis JP, Schmid CH (1998) Summing up evidence: one answer is not always enough. Lancet 351:123-127
-
(1998)
Lancet
, vol.351
, pp. 123-127
-
-
Lau, J.1
Ioannidis, J.P.2
Schmid, C.H.3
-
25
-
-
33646119427
-
Maternal polymorphisms 677C-T and 1298A-C of MTHFR, and 66A-G MTRR genes: Is there any relationship between polymorphisms of the folate pathway, maternal homocysteine levels, and the risk for having a child with Down syndrome?
-
Martinez-Frias ML, Perez B, Desviat LR, Castro M, Leal F, Rodriguez L, Mansilla E, Martinez-Fernandez ML, Bermejo E, Rodriguez-Pinilla E, Prieto D, Ugarte M (2006) Maternal polymorphisms 677C-T and 1298A-C of MTHFR, and 66A-G MTRR genes: is there any relationship between polymorphisms of the folate pathway, maternal homocysteine levels, and the risk for having a child with Down syndrome? Am J Med Genet A 140:987-997
-
(2006)
Am J Med Genet a
, vol.140
, pp. 987-997
-
-
Martinez-Frias, M.L.1
Perez, B.2
Desviat, L.R.3
Castro, M.4
Leal, F.5
Rodriguez, L.6
Mansilla, E.7
Martinez-Fernandez, M.L.8
Bermejo, E.9
Rodriguez-Pinilla, E.10
Prieto, D.11
Ugarte, M.12
-
26
-
-
0037079894
-
MTRR and MTHFR polymorphism: Link to Down syndrome?
-
O'Leary VB, Parle-McDermott A, Molloy AM, Kirke PN, Johnson Z, Conley M, Scott JM, Mills JL (2002) MTRR and MTHFR polymorphism: link to Down syndrome? Am J Med Genet 107:151-155
-
(2002)
Am J Med Genet
, vol.107
, pp. 151-155
-
-
O'Leary, V.B.1
Parle-Mcdermott, A.2
Molloy, A.M.3
Kirke, P.N.4
Johnson, Z.5
Conley, M.6
Scott, J.M.7
Mills, J.L.8
-
27
-
-
33646449190
-
MTHFR C677T and A1298C polymorphisms are risk factors for Down's syndrome in Indian mothers
-
Rai AK, Singh S, Mehta S, Kumar A, Pandey LK, Raman R (2006) MTHFR C677T and A1298C polymorphisms are risk factors for Down's syndrome in Indian mothers. J Hum Genet 51:278-283
-
(2006)
J Hum Genet
, vol.51
, pp. 278-283
-
-
Rai, A.K.1
Singh, S.2
Mehta, S.3
Kumar, A.4
Pandey, L.K.5
Raman, R.6
-
28
-
-
33747873426
-
Analysis of seven maternal polymorphisms of genes involved in homocysteine/folate metabolism and risk of Down syndrome offspring
-
Scala I, Granese B, Sellitto M, Salome S, Sammartino A, Pepe A, Mastroiacovo P, Sebastio G, Andria G (2006) Analysis of seven maternal polymorphisms of genes involved in homocysteine/folate metabolism and risk of Down syndrome offspring. Genet Med 8:409-416
-
(2006)
Genet Med
, vol.8
, pp. 409-416
-
-
Scala, I.1
Granese, B.2
Sellitto, M.3
Salome, S.4
Sammartino, A.5
Pepe, A.6
Mastroiacovo, P.7
Sebastio, G.8
Andria, G.9
-
29
-
-
0033667445
-
Publication and related bias in meta-analysis: Power of statistical tests and prevalence in the literature
-
Sterne JA, Gavaghan D, Egger M (2000) Publication and related bias in meta-analysis: power of statistical tests and prevalence in the literature. J Clin Epidemiol 53:1119-1129
-
(2000)
J Clin Epidemiol
, vol.53
, pp. 1119-1129
-
-
Sterne, J.A.1
Gavaghan, D.2
Egger, M.3
-
30
-
-
0036021040
-
C677T mutation in the 5,10-MTHFR gene and risk of Down syndrome in Italy
-
Stuppia L, Gatta V, Gaspari AR, Antonucci I, Morizio E, Calabrese G, Palka G (2002) C677T mutation in the 5,10-MTHFR gene and risk of Down syndrome in Italy. Eur J Hum Genet 10:388-390
-
(2002)
Eur J Hum Genet
, vol.10
, pp. 388-390
-
-
Stuppia, L.1
Gatta, V.2
Gaspari, A.R.3
Antonucci, I.4
Morizio, E.5
Calabrese, G.6
Palka, G.7
-
31
-
-
0035313224
-
Biological and clinical implications of the MTHFR C677T polymorphism
-
Ueland PM, Hustad S, Schneede J, Refsum H, Vollset SE (2001) Biological and clinical implications of the MTHFR C677T polymorphism. Trends Pharmacol Sci 22:195-201
-
(2001)
Trends Pharmacol Sci
, vol.22
, pp. 195-201
-
-
Ueland, P.M.1
Hustad, S.2
Schneede, J.3
Refsum, H.4
Vollset, S.E.5
-
33
-
-
0031687887
-
A second genetic polymorphism in methylenetetrahydrofolate reductase (MTHFR) associated with decreased enzyme activity
-
Weisberg I, Tran P, Christensen B, Sibani S, Rozen R (1998) A second genetic polymorphism in methylenetetrahydrofolate reductase (MTHFR) associated with decreased enzyme activity. Mol Genet Metab 64:169-172
-
(1998)
Mol Genet Metab
, vol.64
, pp. 169-172
-
-
Weisberg, I.1
Tran, P.2
Christensen, B.3
Sibani, S.4
Rozen, R.5
-
35
-
-
0032856882
-
A common variant in methionine synthase reductase combined with low cobalamin (vitamin B12) increases risk for spina bifida
-
Wilson A, Platt R, Wu Q, Leclerc D, Christensen B, Yang H, Gravel RA, Rozen R (1999) A common variant in methionine synthase reductase combined with low cobalamin (vitamin B12) increases risk for spina bifida. Mol Genet Metab 67:317-323
-
(1999)
Mol Genet Metab
, vol.67
, pp. 317-323
-
-
Wilson, A.1
Platt, R.2
Wu, Q.3
Leclerc, D.4
Christensen, B.5
Yang, H.6
Gravel, R.A.7
Rozen, R.8
-
36
-
-
33745889354
-
Association of methylenetetrahydrofolate reductase (MTHFR) polymorphisms with genetic susceptibility to gastric cancer: A meta-analysis
-
Zintzaras E (2006a) Association of methylenetetrahydrofolate reductase (MTHFR) polymorphisms with genetic susceptibility to gastric cancer: a meta-analysis. J Hum Genet 51:618-624
-
(2006)
J Hum Genet
, vol.51
, pp. 618-624
-
-
Zintzaras, E.1
-
37
-
-
33746792898
-
C677T and A1298C methylenetetrahydrofolate reductase gene polymorphisms in schizophrenia, bipolar disorder and depression: A meta-analysis of genetic association studies
-
Zintzaras E (2006b) C677T and A1298C methylenetetrahydrofolate reductase gene polymorphisms in schizophrenia, bipolar disorder and depression: a meta-analysis of genetic association studies. Psychiatr Genet 16:105-115
-
(2006)
Psychiatr Genet
, vol.16
, pp. 105-115
-
-
Zintzaras, E.1
-
38
-
-
33645472458
-
Methylenetetrahydrofolate reductase gene and susceptibility to breast cancer: A meta-analysis
-
Zintzaras E (2006c). Methylenetetrahydrofolate reductase gene and susceptibility to breast cancer: a meta-analysis. Clin Genet 69:327-336
-
(2006)
Clin Genet
, vol.69
, pp. 327-336
-
-
Zintzaras, E.1
-
39
-
-
34247101730
-
Brain-derived neurotrophic factor gene polymorphisms and schizophrenia: A meta-analysis
-
Zintzaras E (2007) Brain-derived neurotrophic factor gene polymorphisms and schizophrenia: a meta-analysis. Psychiatr Genet 17:69-75
-
(2007)
Psychiatr Genet
, vol.17
, pp. 69-75
-
-
Zintzaras, E.1
-
40
-
-
4744363276
-
Association of paraoxonase 1 gene polymorphisms with risk of Parkinson's disease: A meta-analysis
-
Zintzaras E, Hadjigeorgiou GM (2004) Association of paraoxonase 1 gene polymorphisms with risk of Parkinson's disease: a meta-analysis. J Hum Genet 49:474-481
-
(2004)
J Hum Genet
, vol.49
, pp. 474-481
-
-
Zintzaras, E.1
Hadjigeorgiou, G.M.2
-
41
-
-
15944362595
-
Association between the GLUT1 gene polymorphism and the risk of diabetic nephropathy: A meta-analysis
-
Zintzaras E, Stefanidis I (2005) Association between the GLUT1 gene polymorphism and the risk of diabetic nephropathy: a meta-analysis. J Hum Genet 50:84-91
-
(2005)
J Hum Genet
, vol.50
, pp. 84-91
-
-
Zintzaras, E.1
Stefanidis, I.2
-
42
-
-
34548317291
-
Is 472G/A catechol-O-methyl-transferase gene polymorphism related to panic disorder?
-
Zintzaras E, Sakelaridis N (2007) Is 472G/A catechol-O-methyl-transferase gene polymorphism related to panic disorder? Psychiatr Genet 17:267-273
-
(2007)
Psychiatr Genet
, vol.17
, pp. 267-273
-
-
Zintzaras, E.1
Sakelaridis, N.2
-
43
-
-
23844441200
-
The relationship between C677T methylenetetrahydrofolate reductase gene polymorphism and retinopathy in type 2 diabetes: A meta-analysis
-
Zintzaras E, Chatzoulis DZ, Karabatsas CH, Stefanidis I (2005) The relationship between C677T methylenetetrahydrofolate reductase gene polymorphism and retinopathy in type 2 diabetes: a meta-analysis. J Hum Genet 50:267-275
-
(2005)
J Hum Genet
, vol.50
, pp. 267-275
-
-
Zintzaras, E.1
Chatzoulis, D.Z.2
Karabatsas, C.H.3
Stefanidis, I.4
-
44
-
-
33750090420
-
A meta-analysis of genotypes and haplotypes of methylenetetrahydrofolate reductase gene polymorphisms in acute lymphoblastic leukemia
-
Zintzaras E, Koufakis T, Ziakas PD, Rodopoulou P, Giannouli S, Voulgarelis M (2006a) A meta-analysis of genotypes and haplotypes of methylenetetrahydrofolate reductase gene polymorphisms in acute lymphoblastic leukemia. Eur J Epidemiol 21:501-510
-
(2006)
Eur J Epidemiol
, vol.21
, pp. 501-510
-
-
Zintzaras, E.1
Koufakis, T.2
Ziakas, P.D.3
Rodopoulou, P.4
Giannouli, S.5
Voulgarelis, M.6
-
45
-
-
33750586809
-
Endothelial NO synthase gene polymorphisms and hypertension: A meta-analysis
-
Zintzaras E, Kitsios G, Stefanidis I (2006b) Endothelial NO synthase gene polymorphisms and hypertension: a meta-analysis. Hypertension 48:700-710
-
(2006)
Hypertension
, vol.48
, pp. 700-710
-
-
Zintzaras, E.1
Kitsios, G.2
Stefanidis, I.3
-
46
-
-
33644499201
-
Do alcohol-metabolizing enzyme gene polymorphisms increase the risk of alcoholism and alcoholic liver disease?
-
Zintzaras E, Stefanidis I, Santos M, Vidal F (2006c) Do alcohol-metabolizing enzyme gene polymorphisms increase the risk of alcoholism and alcoholic liver disease? Hepatology 43:352-361
-
(2006)
Hepatology
, vol.43
, pp. 352-361
-
-
Zintzaras, E.1
Stefanidis, I.2
Santos, M.3
Vidal, F.4
-
47
-
-
33847360634
-
BsmI, TaqI, ApaI and FokI polymorphisms in the vitamin D receptor (VDR) gene and the risk of osteoporosis: A meta-analysis
-
Zintzaras E, Rodopoulou P, Koukoulis GN (2006d) BsmI, TaqI, ApaI and FokI polymorphisms in the vitamin D receptor (VDR) gene and the risk of osteoporosis: a meta-analysis. Dis Markers 22:317-326
-
(2006)
Dis Markers
, vol.22
, pp. 317-326
-
-
Zintzaras, E.1
Rodopoulou, P.2
Koukoulis, G.N.3
-
48
-
-
36148965526
-
Methylenetetrahydrofolate reductase gene polymorphism as a risk factor for diabetic nephropathy: A meta-analysis
-
DOI: 10.1007/s10038-007-0189-3
-
Zintzaras E, Uhlig K, Koukoulis GN, Papathanasiou AA, Stefanidis I (2007) Methylenetetrahydrofolate reductase gene polymorphism as a risk factor for diabetic nephropathy: a meta-analysis. J Hum Genet DOI: 10.1007/s10038-007-0189- 3
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(2007)
J Hum Genet
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Zintzaras, E.1
Uhlig, K.2
Koukoulis, G.N.3
Papathanasiou, A.A.4
Stefanidis, I.5
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