-
1
-
-
0027532914
-
Global estimates for prevalence of diabetes mellitus and impaired glucose tolerance in adults
-
1. King H, Rewers M, WHO Ad Hoc Diabetes Reporting Group (1993) Global estimates for prevalence of diabetes mellitus and impaired glucose tolerance in adults. Diabetes Care 16: 157-177
-
(1993)
Diabetes Care
, vol.16
, pp. 157-177
-
-
King, H.1
Rewers, M.2
-
2
-
-
9044243415
-
A genome-wide search for human non-insulin dependent (type 2) diabetes genes reveals a major susceptibility locus on chromosome 2
-
2. Hanis CL, Boerwinkle E, Chakraborty R et al. (1996) A genome-wide search for human non-insulin dependent (type 2) diabetes genes reveals a major susceptibility locus on chromosome 2. Nat Genet 13: 161-166
-
(1996)
Nat Genet
, vol.13
, pp. 161-166
-
-
Hanis, C.L.1
Boerwinkle, E.2
Chakraborty, R.3
-
3
-
-
16044374799
-
Mapping of a gene for type 2 diabetes mellitus associated with an insulin secretion defect by genome scan in Finnish families
-
3. Mahtani MM, Widen E, Lehto M et al. (1996) Mapping of a gene for type 2 diabetes mellitus associated with an insulin secretion defect by genome scan in Finnish families. Nat Genet 14: 90-94
-
(1996)
Nat Genet
, vol.14
, pp. 90-94
-
-
Mahtani, M.M.1
Widen, E.2
Lehto, M.3
-
4
-
-
0025057199
-
Scope and heterogeneous nature of MODY
-
4. Fajans SS (1990) Scope and heterogeneous nature of MODY. Diabetes Care 13: 49-64
-
(1990)
Diabetes Care
, vol.13
, pp. 49-64
-
-
Fajans, S.S.1
-
5
-
-
0028087153
-
Abnormal insulin secretion, not insulin resistance, is the genetic or primary defect of MODY in the RW pedigree
-
5. Herman WH, Fajans SS, Ortiz FJ et al. (1994) Abnormal insulin secretion, not insulin resistance, is the genetic or primary defect of MODY in the RW Pedigree. Diabetes 43: 40-46
-
(1994)
Diabetes
, vol.43
, pp. 40-46
-
-
Herman, W.H.1
Fajans, S.S.2
Ortiz, F.J.3
-
6
-
-
10544236911
-
Mutations in the hepatocyte nuclear factor-4α gene in maturity-onset diabetes of the young (MODY1)
-
6. Yamagata K, Furuta H, Oda N et al. (1996) Mutations in the hepatocyte nuclear factor-4α gene in maturity-onset diabetes of the young (MODY1). Nature 384: 458-460
-
(1996)
Nature
, vol.384
, pp. 458-460
-
-
Yamagata, K.1
Furuta, H.2
Oda, N.3
-
7
-
-
0032792499
-
Characterization of glucokinase mutations associated with maturity-onset diabetes of the young type 2 (MODY2): Different glucokinase defects lead to a common phenotype
-
7. Miller SP, Anand GR, Karschnia EJ, Bell GI, LaPorte DC, Lange AJ (1999) Characterization of glucokinase mutations associated with maturity-onset diabetes of the young type 2 (MODY2): different glucokinase defects lead to a common phenotype. Diabetes 48: 1645-1651
-
(1999)
Diabetes
, vol.48
, pp. 1645-1651
-
-
Miller, S.P.1
Anand, G.R.2
Karschnia, E.J.3
Bell, G.I.4
LaPorte, D.C.5
Lange, A.J.6
-
8
-
-
10544249874
-
Mutations in the hepatocyte nuclear factor-1α gene in maturity-onset diabetes of the young (MODY3)
-
8. Yamagata K, Oda N, Kaisaki PJ et al. (1996) Mutations in the hepatocyte nuclear factor-1α gene in maturity-onset diabetes of the young (MODY3). Nature 384: 455-458
-
(1996)
Nature
, vol.384
, pp. 455-458
-
-
Yamagata, K.1
Oda, N.2
Kaisaki, P.J.3
-
10
-
-
0031453186
-
Mutation in hepatocyte nuclear factor-1 beta gene (TCF2) associated with MODY
-
10. Horikawa Y, Iwasaki N, Hara M et al. (1997) Mutation in hepatocyte nuclear factor-1 beta gene (TCF2) associated with MODY. Nat Genet 17: 384-385
-
(1997)
Nat Genet
, vol.17
, pp. 384-385
-
-
Horikawa, Y.1
Iwasaki, N.2
Hara, M.3
-
11
-
-
0030695445
-
The maturity-onset diabetes of the young (MODY1) transcription factor HNF4α regulates expression of genes required for glucose transport and metabolism
-
11. Stöffel M, Duncan SA (1997) The maturity-onset diabetes of the young (MODY1) transcription factor HNF4α regulates expression of genes required for glucose transport and metabolism. Proc Natl Acad Sci USA 94: 13209-13214
-
(1997)
Proc Natl Acad Sci USA
, vol.94
, pp. 13209-13214
-
-
Stöffel, M.1
Duncan, S.A.2
-
12
-
-
0001418036
-
Hepatocyte nuclear factor 4 (HNF4)
-
Tronche F, Yaniv M (eds). Landes, Austin
-
12. Sladek FM (1994) Hepatocyte nuclear factor 4 (HNF4). In: Tronche F, Yaniv M (eds) Liver Gene Expression. Landes, Austin, pp 207-230
-
(1994)
Liver Gene Expression
, pp. 207-230
-
-
Sladek, F.M.1
-
13
-
-
0031914679
-
Maturity-onset diabetes of the young: Clinical heterogeneity explained by genetic heterogeneity
-
13. Hattersley AT (1998) Maturity-onset diabetes of the young: clinical heterogeneity explained by genetic heterogeneity. Diabet Med 15: 15-24
-
(1998)
Diabet Med
, vol.15
, pp. 15-24
-
-
Hattersley, A.T.1
-
14
-
-
8244219694
-
Identification of nine novel mutations in the hepatocyte nuclear factor 1 alpha gene associated with maturity-onset diabetes of the young (MODY3)
-
14. Vaxillaire M, Rouard M, Yamagata K et al. (1997) Identification of nine novel mutations in the hepatocyte nuclear factor 1 alpha gene associated with maturity-onset diabetes of the young (MODY3). Hum Mol Genet 6: 583-586
-
(1997)
Hum Mol Genet
, vol.6
, pp. 583-586
-
-
Vaxillaire, M.1
Rouard, M.2
Yamagata, K.3
-
15
-
-
15144351715
-
Mutations in the hepatocyte nuclear factor-1-alpha gene in MODY and early-onset NIDDM: Evidence for a mutational hotspot in exon 4
-
15. Kaisaki PJ, Menzel S, Lindner T et al. (1997) Mutations in the hepatocyte nuclear factor-1-alpha gene in MODY and early-onset NIDDM: evidence for a mutational hotspot in exon 4. Diabetes 46: 528-535
-
(1997)
Diabetes
, vol.46
, pp. 528-535
-
-
Kaisaki, P.J.1
Menzel, S.2
Lindner, T.3
-
16
-
-
15444352146
-
Novel MODY3 mutations in the hepatocyte nuclear factor-1-alpha gene: Evidence for a hyperexcitability of pancreatic beta-cells to intravenous secretagogues in a glucose tolerant carrier of a P447L mutation
-
16. Hansen T, Eiberg H, Rouard M et al. (1997) Novel MODY3 mutations in the hepatocyte nuclear factor-1-alpha gene: evidence for a hyperexcitability of pancreatic beta-cells to intravenous secretagogues in a glucose tolerant carrier of a P447L mutation. Diabetes 46: 726-730
-
(1997)
Diabetes
, vol.46
, pp. 726-730
-
-
Hansen, T.1
Eiberg, H.2
Rouard, M.3
-
17
-
-
0030798412
-
Maturity-onset diabetes of the young due to a mutation in the hepatocyte nuclear factor-4-alpha binding site in the promoter of the hepatocyte nuclear factor-1-alpha gene
-
17. Gragnoli C, Lindner T, Cockburn BN, Kaisaki PJ, Gragnoli F, Marozzi G, Bell GI (1997) Maturity-onset diabetes of the young due to a mutation in the hepatocyte nuclear factor-4-alpha binding site in the promoter of the hepatocyte nuclear factor-1-alpha gene. Diabetes 46: 1648-1651
-
(1997)
Diabetes
, vol.46
, pp. 1648-1651
-
-
Gragnoli, C.1
Lindner, T.2
Cockburn, B.N.3
Kaisaki, P.J.4
Gragnoli, F.5
Marozzi, G.6
Bell, G.I.7
-
18
-
-
0031447766
-
A rapid screening method for hepatocyte nuclear factor 1 alpha frameshift mutations; prevalence in maturity-onset diabetes of the young and late-onset non-insulin dependent diabetes
-
18. Frayling TM, Bulman MP, Appleton M, Hattersley AT, Ellard S (1997) A rapid screening method for hepatocyte nuclear factor 1 alpha frameshift mutations; prevalence in maturity-onset diabetes of the young and late-onset non-insulin dependent diabetes. Hum Genet 101: 351-354
-
(1997)
Hum Genet
, vol.101
, pp. 351-354
-
-
Frayling, T.M.1
Bulman, M.P.2
Appleton, M.3
Hattersley, A.T.4
Ellard, S.5
-
19
-
-
14444278300
-
Mutations in the hepatocyte nuclear factor-1-alpha gene are a common cause of maturity-onset diabetes of the young in the U.K
-
19. Frayling TM, Bulman MP, Ellard S et al.(1997) Mutations in the hepatocyte nuclear factor-1-alpha gene are a common cause of maturity-onset diabetes of the young in the U.K. Diabetes 46: 720-725
-
(1997)
Diabetes
, vol.46
, pp. 720-725
-
-
Frayling, T.M.1
Bulman, M.P.2
Ellard, S.3
-
20
-
-
0030779004
-
Hepatic function in a family with a nonsense mutation (R154X) in the hepatocyte nuclear factor-4-alpha/MODY1 gene
-
20. Lindner T, Gragnoli C, Furuta H et al. (1997) Hepatic function in a family with a nonsense mutation (R154X) in the hepatocyte nuclear factor-4-alpha/MODY1 gene. J Clin Invest 100: 1400-1405
-
(1997)
J Clin Invest
, vol.100
, pp. 1400-1405
-
-
Lindner, T.1
Gragnoli, C.2
Furuta, H.3
-
21
-
-
0000309667
-
Organization and partial sequence of the hepatocyte nuclear factor-4α/ MODY1 gene and identification of a missense mutation, R127W, in a Japanese family with MODY
-
21. Furuta H, Iwasaki N, Oda N et al. (1997) Organization and partial sequence of the hepatocyte nuclear factor-4α/ MODY1 gene and identification of a missense mutation, R127W, in a Japanese family with MODY. Diabetes 46: 1652-1657
-
(1997)
Diabetes
, vol.46
, pp. 1652-1657
-
-
Furuta, H.1
Iwasaki, N.2
Oda, N.3
-
22
-
-
0032006573
-
A missense mutation in hepatocyte nuclear factor-4α resulting in a reduced transactivation activity, in human late-onset non-insulin-dependent diabetes mellitus
-
22. Hani EH, Suaud L, Boutin P et al. (1998) A missense mutation in hepatocyte nuclear factor-4α resulting in a reduced transactivation activity, in human late-onset non-insulin-dependent diabetes mellitus. J Clin Invest 101: 521-526
-
(1998)
J Clin Invest
, vol.101
, pp. 521-526
-
-
Hani, E.H.1
Suaud, L.2
Boutin, P.3
-
23
-
-
0030850883
-
A missense mutation in the hepatocyte nuclear factor 4 alpha gene in a UK pedigree with maturity-onset diabetes of the young
-
23. Bulman MP, Dronsfield MJ, Frayling T et al. (1997) A missense mutation in the hepatocyte nuclear factor 4 alpha gene in a UK pedigree with maturity-onset diabetes of the young. Diabetologia 40: 859-862
-
(1997)
Diabetologia
, vol.40
, pp. 859-862
-
-
Bulman, M.P.1
Dronsfield, M.J.2
Frayling, T.3
-
24
-
-
0032955956
-
A novel Phe75fsdelT mutation in the hepatocyte nuclear factor-4alpha gene in a Danish pedigree with maturity onset diabetes of the young
-
24. Moller AM, Dalgaard LT, Ambye L et al. (1999) A novel Phe75fsdelT mutation in the hepatocyte nuclear factor-4alpha gene in a Danish pedigree with maturity onset diabetes of the young. J Clin Endocrinol Metab 84: 367-369
-
(1999)
J Clin Endocrinol Metab
, vol.84
, pp. 367-369
-
-
Moller, A.M.1
Dalgaard, L.T.2
Ambye, L.3
-
25
-
-
0032758592
-
Identification of new mutations in the hepatocyte nuclear factor 4alpha gene among families with early onset type 2 diabetes mellitus
-
25. Malecki MT, Yang Y, Antonellis A et al. (1999) Identification of new mutations in the hepatocyte nuclear factor 4alpha gene among families with early onset type 2 diabetes mellitus. Diabet Med 16: 193-200
-
(1999)
Diabet Med
, vol.16
, pp. 193-200
-
-
Malecki, M.T.1
Yang, Y.2
Antonellis, A.3
-
26
-
-
0030897631
-
Linkage of genetic markers on human chromosomes 20 and 12 to NIDDM in Caucasian sib pairs with a history of diabetic nephropathy
-
26. Bowden DW, Sale M, Howard TD et al. (1997) Linkage of genetic markers on human chromosomes 20 and 12 to NIDDM in Caucasian sib pairs with a history of diabetic nephropathy. Diabetes 46: 882-886
-
(1997)
Diabetes
, vol.46
, pp. 882-886
-
-
Bowden, D.W.1
Sale, M.2
Howard, T.D.3
-
27
-
-
0030907295
-
New susceptibility locus for NIDDM is localized to human chromosome 20q
-
27. Ji L, Malecki M, Warram JH, Yang Y, Rich SS, Krolewski AS (1997) New susceptibility locus for NIDDM is localized to human chromosome 20q. Diabetes 46: 876-881
-
(1997)
Diabetes
, vol.46
, pp. 876-881
-
-
Ji, L.1
Malecki, M.2
Warram, J.H.3
Yang, Y.4
Rich, S.S.5
Krolewski, A.S.6
-
28
-
-
0030766446
-
A susceptibility locus for early-onset non-insulin dependent (type 2) diabetes mellitus maps to chromosome 20q, proximal to the phophoenolpyruvate carboxykinase gene
-
28. Zouali H, Hani EH, Philippi A et al. (1997) A susceptibility locus for early-onset non-insulin dependent (type 2) diabetes mellitus maps to chromosome 20q, proximal to the phophoenolpyruvate carboxykinase gene. Hum Mol Genet 6: 1401-1408
-
(1997)
Hum Mol Genet
, vol.6
, pp. 1401-1408
-
-
Zouali, H.1
Hani, E.H.2
Philippi, A.3
-
29
-
-
13044277561
-
Type 2 diabetes: Evidence for linkage on chromosome 20 in 716 Finnish affected sibpairs
-
29. Ghosh S, Watanabe RM, Hauser E et al. (1999) Type 2 diabetes: evidence for linkage on chromosome 20 in 716 Finnish affected sibpairs. Proc Natl Acad Sci USA 96: 2198-2203
-
(1999)
Proc Natl Acad Sci USA
, vol.96
, pp. 2198-2203
-
-
Ghosh, S.1
Watanabe, R.M.2
Hauser, E.3
-
30
-
-
0000950303
-
Construction of a physical map of chromosome 20q12-13.1 and linkage disequilibrium analysis in diabetic nephropathy patients
-
30. Price JA, Brewer CS, Howard TD et al. (1997) Construction of a physical map of chromosome 20q12-13.1 and linkage disequilibrium analysis in diabetic nephropathy patients. Am J Hum Genet 61[Suppl]:A241 (Abstract)
-
(1997)
Am J Hum Genet
, vol.61
, Issue.SUPPL.
-
-
Price, J.A.1
Brewer, C.S.2
Howard, T.D.3
-
31
-
-
0031832935
-
A detailed physical and transcriptional map of the region of chromosome 20 that is deleted in myeloproliferative disorders and refinement of the common deleted region
-
31. Bench AJ, Aldred MA, Humphray SJ et al. (1998) A detailed physical and transcriptional map of the region of chromosome 20 that is deleted in myeloproliferative disorders and refinement of the common deleted region. Genomics 49: 351-362
-
(1998)
Genomics
, vol.49
, pp. 351-362
-
-
Bench, A.J.1
Aldred, M.A.2
Humphray, S.J.3
-
32
-
-
9244258538
-
A yeast artificial chromosome-based map of the region of chromosome 20 containing the diabetes-susceptibility gene, MODY1, and a myeloid leukemia related gene
-
32. Stoffel M, Le Beau MM, Espinosa R et al. (1996) A yeast artificial chromosome-based map of the region of chromosome 20 containing the diabetes-susceptibility gene, MODY1, and a myeloid leukemia related gene. Proc Natl Acad Sci USA 93: 3937-3941
-
(1996)
Proc Natl Acad Sci USA
, vol.93
, pp. 3937-3941
-
-
Stoffel, M.1
Le Beau, M.M.2
Espinosa, R.3
-
33
-
-
0033385498
-
A physical map of the 20q12-13.1 region associated with type 2 diabetes
-
33. Price JA, Brewer CS, Howard TD et al. (1999) A physical map of the 20q12-13.1 region associated with Type 2 diabetes. Genomics 62: 208-215
-
(1999)
Genomics
, vol.62
, pp. 208-215
-
-
Price, J.A.1
Brewer, C.S.2
Howard, T.D.3
-
34
-
-
15444360683
-
PowerBLAST: A new network BLAST application for interactive or automated sequence analysis and annotation
-
34. Zhang J, Madden TL (1997) PowerBLAST: a new network BLAST application for interactive or automated sequence analysis and annotation. Genome Res 7: 649-656
-
(1997)
Genome Res
, vol.7
, pp. 649-656
-
-
Zhang, J.1
Madden, T.L.2
-
35
-
-
0023867357
-
Sterol-dependent repression of low density lipoprotein receptor promoter mediated by 16-base pair sequence adjacent to binding site for the transcription factor Sp1
-
35. Dawson PA, Hofmann SL, van der Westhuyzen DR, Sudhof TC, Brown MS, Goldstein JL (1988) Sterol-dependent repression of low density lipoprotein receptor promoter mediated by 16-base pair sequence adjacent to binding site for the transcription factor Sp1. J Biol Chem 263: 3372-3379
-
(1988)
J Biol Chem
, vol.263
, pp. 3372-3379
-
-
Dawson, P.A.1
Hofmann, S.L.2
Van Der Westhuyzen, D.R.3
Sudhof, T.C.4
Brown, M.S.5
Goldstein, J.L.6
-
36
-
-
0021770607
-
Functional analysis of the steroid hormone control region of mouse mammary tumor virus
-
36. Lee F, Hall CV, Ringold GM, Dobson DE, Luh J, Jacob PE (1984) Functional analysis of the steroid hormone control region of mouse mammary tumor virus. Nucleic Acids Res 12: 4191-4206
-
(1984)
Nucleic Acids Res
, vol.12
, pp. 4191-4206
-
-
Lee, F.1
Hall, C.V.2
Ringold, G.M.3
Dobson, D.E.4
Luh, J.5
Jacob, P.E.6
-
37
-
-
0025527807
-
A dictionary of transcription control sequences
-
37. Locker J, Buzard G (1990) A dictionary of transcription control sequences. DNA Seq 1: 3-11
-
(1990)
DNA Seq
, vol.1
, pp. 3-11
-
-
Locker, J.1
Buzard, G.2
-
38
-
-
0031802866
-
Exclusion of the hepatocyte nuclear factor 4α as a candidate gene for late-onset NIDDM linked with chromosome 20q
-
38. Malecki MT, Antonellis A, Casey P et al. (1998) Exclusion of the hepatocyte nuclear factor 4α as a candidate gene for late-onset NIDDM linked with chromosome 20q. Diabetes 46: 970-972
-
(1998)
Diabetes
, vol.46
, pp. 970-972
-
-
Malecki, M.T.1
Antonellis, A.2
Casey, P.3
-
39
-
-
0030798068
-
Studies of the genetic variability of the coding region of the hepatocyte nuclear factor-4α in Caucasians with maturity onset NIDDM
-
39. Moller AM, Urhammer SA, Dalgaard LT et al. (1997) Studies of the genetic variability of the coding region of the hepatocyte nuclear factor-4α in Caucasians with maturity onset NIDDM. Diabetologia 40: 980-983
-
(1997)
Diabetologia
, vol.40
, pp. 980-983
-
-
Moller, A.M.1
Urhammer, S.A.2
Dalgaard, L.T.3
-
40
-
-
0030590359
-
Isolation and characterization of a third isoform of human hepatocyte nuclear factor 4
-
40. Kritis AA, Argyrokastritis A, Moschonas NK et al. (1996) Isolation and characterization of a third isoform of human hepatocyte nuclear factor 4. Gene 173: 275-280
-
(1996)
Gene
, vol.173
, pp. 275-280
-
-
Kritis, A.A.1
Argyrokastritis, A.2
Moschonas, N.K.3
-
41
-
-
46149139074
-
Promoter-specific activation of RNA polymerase II transcription by Sp1
-
41. Kagonaga JT, Jones KA, Tijan R (1986) Promoter-specific activation of RNA polymerase II transcription by Sp1. Trends Biochem Sci 11: 20-23
-
(1986)
Trends Biochem Sci
, vol.11
, pp. 20-23
-
-
Kagonaga, J.T.1
Jones, K.A.2
Tijan, R.3
-
42
-
-
0026455188
-
Functional analysis of the human platelet-derived growth factor A-chain promoter region
-
42. Lin X, Wang Z, Gu L, Deuel TF (1992) Functional analysis of the human platelet-derived growth factor A-chain promoter region. J Biol Chem 267: 25614-25619
-
(1992)
J Biol Chem
, vol.267
, pp. 25614-25619
-
-
Lin, X.1
Wang, Z.2
Gu, L.3
Deuel, T.F.4
-
43
-
-
0025827852
-
A cluster of four Sp1 binding sites required for efficient expression of the human insulin receptor gene
-
43. Araki E, Murakami T, Shirotani T et al. (1991) A cluster of four Sp1 binding sites required for efficient expression of the human insulin receptor gene. J Biol Chem 266: 3944-3948
-
(1991)
J Biol Chem
, vol.266
, pp. 3944-3948
-
-
Araki, E.1
Murakami, T.2
Shirotani, T.3
-
44
-
-
0030795465
-
Binding of phosphorylated Sp1 protein to tandem Sp1 binding sites regulates α2 integrin gene promoter activity
-
44. Zutter MM, Ryan EE, Painter AD (1997) Binding of phosphorylated Sp1 protein to tandem Sp1 binding sites regulates α2 integrin gene promoter activity. Blood 90: 678-689
-
(1997)
Blood
, vol.90
, pp. 678-689
-
-
Zutter, M.M.1
Ryan, E.E.2
Painter, A.D.3
-
45
-
-
0031462103
-
Transcriptional regulation by the Sp family proteins
-
45. Lania L, Majello B, De Luca P (1997) Transcriptional regulation by the Sp family proteins. Int J Biochem Cell Biol 29: 1313-1323
-
(1997)
Int J Biochem Cell Biol
, vol.29
, pp. 1313-1323
-
-
Lania, L.1
Majello, B.2
De Luca, P.3
-
46
-
-
0031802977
-
MODY1 mutation Q268X in hepatocyte nuclear factor 4a allows for dimerization in solution but causes abnormal subcellular localization
-
46. Sladek FM, Dallas-Yang Q, Nepomuceno L (1998) MODY1 mutation Q268X in hepatocyte nuclear factor 4a allows for dimerization in solution but causes abnormal subcellular localization. Diabetes 47: 985-990
-
(1998)
Diabetes
, vol.47
, pp. 985-990
-
-
Sladek, F.M.1
Dallas-Yang, Q.2
Nepomuceno, L.3
-
47
-
-
0033028606
-
Functional characterization of the MODY1 gene mutations HNF4(R127W), HNF4 (V255M), and HNF4(E276Q)
-
47. Navas MA, Munoz-Elias EJ, Kim J, Shih D, Stoffel M (1999) Functional characterization of the MODY1 gene mutations HNF4(R127W), HNF4 (V255M), and HNF4(E276Q). Diabetes 48: 1459-1465
-
(1999)
Diabetes
, vol.48
, pp. 1459-1465
-
-
Navas, M.A.1
Munoz-Elias, E.J.2
Kim, J.3
Shih, D.4
Stoffel, M.5
-
48
-
-
0027434131
-
How sensitive is PCRSSCP?
-
48. Hayashi K, Yandell DW (1993) How sensitive is PCRSSCP? Hum Mutat 2: 338-346
-
(1993)
Hum Mutat
, vol.2
, pp. 338-346
-
-
Hayashi, K.1
Yandell, D.W.2
|