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Results: 19

1.

HGVbase: a human sequence variation database emphasizing data quality and a broad spectrum of data sources.

Fredman D, Siegfried M, Yuan YP, Bork P, Lehväslaiho H, Brookes AJ.

Nucleic Acids Res. 2002 Jan 1;30(1):387-91.

PMID:
11752345
[PubMed - indexed for MEDLINE]
Free PMC Article
2.

[Introduction to Go! Poly, a human genome polymorphism database].

Chen W, Zhang G, Zhang S.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2001 Dec;18(6):482-5. Review. Chinese.

PMID:
11774222
[PubMed - indexed for MEDLINE]
3.

[Single nucleotide polymorphisms(SNPs)and SNP databases].

Gu HF.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2001 Dec;18(6):479-81. Review. Chinese.

PMID:
11774221
[PubMed - indexed for MEDLINE]
4.

Advances in the Exon-Intron Database (EID).

Shepelev V, Fedorov A.

Brief Bioinform. 2006 Jun;7(2):178-85. Epub 2006 Mar 9. Review.

PMID:
16772261
[PubMed - indexed for MEDLINE]
Free Article
5.

Genome and genetic resources from the Cancer Genome Anatomy Project.

Riggins GJ, Strausberg RL.

Hum Mol Genet. 2001 Apr;10(7):663-7. Review.

PMID:
11257097
[PubMed - indexed for MEDLINE]
Free Article
6.

Using genetic variation to study human disease.

Taylor JG, Choi EH, Foster CB, Chanock SJ.

Trends Mol Med. 2001 Nov;7(11):507-12. Review.

PMID:
11689336
[PubMed - indexed for MEDLINE]
7.

Mutation databases and other online sites as a resource for transfusion medicine: history and attributes.

Blumenfeld OO.

Transfus Med Rev. 2002 Apr;16(2):103-14. Review.

PMID:
11941573
[PubMed - indexed for MEDLINE]
8.

DECIPHER: web-based, community resource for clinical interpretation of rare variants in developmental disorders.

Swaminathan GJ, Bragin E, Chatzimichali EA, Corpas M, Bevan AP, Wright CF, Carter NP, Hurles ME, Firth HV.

Hum Mol Genet. 2012 Oct 15;21(R1):R37-44. Epub 2012 Sep 8. Review.

PMID:
22962312
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

Decoding the human genome sequence.

Bentley DR.

Hum Mol Genet. 2000 Oct;9(16):2353-8. Review.

PMID:
11005789
[PubMed - indexed for MEDLINE]
Free Article
10.

Sequence variation and disease in the wake of the draft human genome.

Goodstadt L, Ponting CP.

Hum Mol Genet. 2001 Oct 1;10(20):2209-14. Review.

PMID:
11673403
[PubMed - indexed for MEDLINE]
Free Article
11.

Searching for candidate genes in the new millennium.

Bleck O, McGrath JA, South AP.

Clin Exp Dermatol. 2001 May;26(3):279-83. Review.

PMID:
11422176
[PubMed - indexed for MEDLINE]
12.

Relevance of the Human Genome Project to inherited metabolic disease.

Burn J.

J Inherit Metab Dis. 1994;17(4):421-9. Review.

PMID:
7967492
[PubMed - indexed for MEDLINE]
13.

[Genome information database].

Minoshima S, Shimizu N.

Tanpakushitsu Kakusan Koso. 1997 Dec;42(17 Suppl):3038-45. Review. Japanese. No abstract available.

PMID:
9455231
[PubMed - indexed for MEDLINE]
14.

Integration of genome data and protein structures: prediction of protein folds, protein interactions and "molecular phenotypes" of single nucleotide polymorphisms.

Sunyaev S, Lathe W 3rd, Bork P.

Curr Opin Struct Biol. 2001 Feb;11(1):125-30. Review.

PMID:
11179902
[PubMed - indexed for MEDLINE]
15.

Strategies in complex disease mapping.

Johnson GC, Todd JA.

Curr Opin Genet Dev. 2000 Jun;10(3):330-4. Review.

PMID:
10826983
[PubMed - indexed for MEDLINE]
16.

Central mutation databases--a review.

Porter CJ, Talbot CC, Cuticchia AJ.

Hum Mutat. 2000;15(1):36-44. Review.

PMID:
10612820
[PubMed - indexed for MEDLINE]
17.

[Genetic information database].

Minoshima S, Shimizu N.

Tanpakushitsu Kakusan Koso. 1996 Nov;41(15 Suppl):2464-77. Review. Japanese. No abstract available.

PMID:
8952411
[PubMed - indexed for MEDLINE]
18.

Databases of human hemoglobin variants and other resources at the globin gene server.

Hardison RC, Chui DH, Riemer C, Giardine B, Lehväslaiho H, Wajcman H, Miller W.

Hemoglobin. 2001 May;25(2):183-93. Review.

PMID:
11480780
[PubMed - indexed for MEDLINE]
19.

Submission of nucleotide sequence data to EMBL/GenBank/DDBJ.

Tuli MA, Flores TP, Cameron GN.

Mol Biotechnol. 1996 Aug;6(1):47-51. Review.

PMID:
8887360
[PubMed - indexed for MEDLINE]

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