157 related articles for article (PubMed ID: 21992487)
1. Come together, right now!
Baxter K; Terry SF
Genet Test Mol Biomarkers; 2011 Oct; 15(10):665-6. PubMed ID: 21992487
[No Abstract] [Full Text] [Related]
2. The challenge of using SNPs in the understanding and treatment of disease.
Schifreen RS; Storts DR; Buller AM
Biotechniques; 2002 Jun; Suppl():14-6, 18, 20-1. PubMed ID: 12083392
[No Abstract] [Full Text] [Related]
3. Introduction to SNPs: discovery of markers for disease.
Weiner MP; Hudson TJ
Biotechniques; 2002 Jun; Suppl():4-7, 10, 12-3. PubMed ID: 12083396
[No Abstract] [Full Text] [Related]
4. Share alike.
Nature; 2012 Oct; 490(7419):143-4. PubMed ID: 23066546
[No Abstract] [Full Text] [Related]
5. [Personalized genetic analysis].
Schenk M
Dtsch Med Wochenschr; 2011 Jul; 136(27):p21. PubMed ID: 21809269
[No Abstract] [Full Text] [Related]
6. Exome and whole-genome sequencing for gene discovery: the future is now!
Majewski J; Rosenblatt DS
Hum Mutat; 2012 Apr; 33(4):591-2. PubMed ID: 22411407
[No Abstract] [Full Text] [Related]
7. Systems approaches for pharmacogenetics and pharmacogenomics.
Bader JS
Pharmacogenomics; 2008 Mar; 9(3):257-62. PubMed ID: 18303961
[No Abstract] [Full Text] [Related]
8. [Towards a national standardisation of NGS studies in the diagnosis of myopathies].
Krahn M; Cerino M; Campana-Salort E; Cossée M
Med Sci (Paris); 2017 Nov; 33 Hors série n°1():30-33. PubMed ID: 29139383
[No Abstract] [Full Text] [Related]
9. New world data.
Biotechniques; 2009 Nov; 47(5):897. PubMed ID: 20043378
[No Abstract] [Full Text] [Related]
10. Forensic DNA and bioinformatics.
Bianchi L; Liò P
Brief Bioinform; 2007 Mar; 8(2):117-28. PubMed ID: 17384432
[TBL] [Abstract][Full Text] [Related]
11. The resequencing imperative.
Topol EJ; Frazer KA
Nat Genet; 2007 Apr; 39(4):439-40. PubMed ID: 17392801
[No Abstract] [Full Text] [Related]
12. Next-generation sequencing approaches for genetic mapping of complex diseases.
Casals F; Idaghdour Y; Hussin J; Awadalla P
J Neuroimmunol; 2012 Jul; 248(1-2):10-22. PubMed ID: 22285396
[TBL] [Abstract][Full Text] [Related]
13. Next generation sequencing: the technology we need in pediatric laboratories?
Couderc R; Jonard L; Louha M
Clin Biochem; 2011 May; 44(7):514-515. PubMed ID: 22036354
[No Abstract] [Full Text] [Related]
14. [Introduction to human genome sequencing in diagnostics].
Piatkowski J; Skalniak A; Bodzioch M; Pach D; Hubalewska-Dydejczyk A
Przegl Lek; 2013; 70(7):458-62. PubMed ID: 24167948
[TBL] [Abstract][Full Text] [Related]
15. [Exome sequencing applied to monogenic disorders].
Criqui A; Baulande S
Med Sci (Paris); 2010 May; 26(5):452-4. PubMed ID: 20510136
[No Abstract] [Full Text] [Related]
16. Genetics. No longer de-identified.
McGuire AL; Gibbs RA
Science; 2006 Apr; 312(5772):370-1. PubMed ID: 16627725
[No Abstract] [Full Text] [Related]
17. [Sequencing technology in gene diagnosis and its application].
Yibin G
Yi Chuan; 2014 Nov; 36(11):1121-30. PubMed ID: 25567870
[TBL] [Abstract][Full Text] [Related]
18. [Do we know our heritage? The Danish Society of Medical Genetics].
Kruse TA
Ugeskr Laeger; 2003 Mar; 165(12):1244. PubMed ID: 12701294
[No Abstract] [Full Text] [Related]
19. The relevance of alternative RNA splicing to pharmacogenomics.
Bracco L; Kearsey J
Trends Biotechnol; 2003 Aug; 21(8):346-53. PubMed ID: 12902171
[TBL] [Abstract][Full Text] [Related]
20. Great expectations: using massively parallel sequencing to solve inherited disorders.
Corbett M; Gecz J
Expert Rev Mol Diagn; 2010 Oct; 10(7):833-6. PubMed ID: 20964599
[No Abstract] [Full Text] [Related]
[Next] [New Search]