These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

146 related articles for article (PubMed ID: 26447529)

  • 1. Your DNA is not your diagnosis: getting diagnoses right following secondary genomic findings.
    Murray MF
    Genet Med; 2016 Aug; 18(8):765-7. PubMed ID: 26447529
    [No Abstract]   [Full Text] [Related]  

  • 2. DNA damage repair gene mutation testing and genetic counseling in men with/without prostate cancer: a systematic review.
    Armstrong N; Quek RG; Ryder S; Ross J; Buksnys T; Forbes C; Fox KM; Castro E
    Future Oncol; 2021 Mar; 17(7):853-864. PubMed ID: 33263430
    [No Abstract]   [Full Text] [Related]  

  • 3. Value of renal gene panel diagnostics in adults waiting for kidney transplantation due to undetermined end-stage renal disease.
    Ottlewski I; Münch J; Wagner T; Schönauer R; Bachmann A; Weimann A; Hentschel J; Lindner TH; Seehofer D; Bergmann C; Jamra RA; Halbritter J
    Kidney Int; 2019 Jul; 96(1):222-230. PubMed ID: 31027891
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Probability of positive genetic testing in patients diagnosed with pheochromocytoma and paraganglioma: Criteria beyond a family history.
    Alobuia WM; Ammar S; Tyagi M; Ghosh C; Gunda V; Annes JP; Kebebew E
    Surgery; 2021 Feb; 169(2):298-301. PubMed ID: 33023754
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Hereditary hemochromatosis: detection of C282Y and H63D mutations in HFE gene by means of guthrie cards in population of Czech Republic.
    Cimburova M; Putova I; Provaznikova H; Horak J
    Genet Epidemiol; 2002 Oct; 23(3):260-3. PubMed ID: 12384978
    [TBL] [Abstract][Full Text] [Related]  

  • 6. To know or not to know the genomic sequence of a fetus.
    Netzer C; Schmitz D; Henn W
    Nat Rev Genet; 2012 Oct; 13(10):676-7. PubMed ID: 22945393
    [No Abstract]   [Full Text] [Related]  

  • 7. Presymptomatic tests in Huntington's disease and dominant ataxias.
    Cannella M; Simonelli M; D'Alessio C; Pierelli F; Ruggieri S; Squitieri F
    Neurol Sci; 2001 Feb; 22(1):55-6. PubMed ID: 11487199
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Prenatal diagnosis and genetic counseling of X-linked Alport syndrome in China].
    Zhang HW; Ding J; Wang F; Yang HX
    Zhonghua Er Ke Za Zhi; 2007 Jul; 45(7):484-9. PubMed ID: 17953801
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mutation analysis of the N-methyl-D-aspartate receptor NR1 subunit gene (GRIN1) in schizophrenia.
    Sakurai K; Toru M; Yamakawa-Kobayashi K; Arinami T
    Neurosci Lett; 2000 Dec; 296(2-3):168-70. PubMed ID: 11109007
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Utility of a Genetic Screening Panel in Patients With Suspected Inherited Retinal Dystrophies.
    McGowan H; Madreperla OR; Snyder AL; Fine HF
    Ophthalmic Surg Lasers Imaging Retina; 2020 Jun; 51(6):338-345. PubMed ID: 32579692
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The "New Genetics" in Clinical Practice: A Brief Primer.
    Milunsky A
    J Am Board Fam Med; 2017; 30(3):377-379. PubMed ID: 28484071
    [TBL] [Abstract][Full Text] [Related]  

  • 12. More breast cancer patients prefer BRCA-mutation testing without prior face-to-face genetic counseling.
    Sie AS; van Zelst-Stams WA; Spruijt L; Mensenkamp AR; Ligtenberg MJ; Brunner HG; Prins JB; Hoogerbrugge N
    Fam Cancer; 2014 Jun; 13(2):143-51. PubMed ID: 24068317
    [TBL] [Abstract][Full Text] [Related]  

  • 13. BRCA1-BRCA2 mutation analysis results in 910 individuals: Mutation distribution and 8 novel mutations.
    Solmaz AE; Onay H; Yeniay L; Gökmen E; Özdemir N; Alanyalı S; Oktay A; Özsaran Z; Kapkaç M; Özkınay F
    Cancer Genet; 2020 Feb; 241():20-24. PubMed ID: 31954625
    [No Abstract]   [Full Text] [Related]  

  • 14. Why mutation analysis does not always predict clinical consequences: explanations in the era of genomics.
    Scriver CR
    J Pediatr; 2002 May; 140(5):502-6. PubMed ID: 12032513
    [No Abstract]   [Full Text] [Related]  

  • 15. Establishing an EGFR mutation screening service for non-small cell lung cancer - sample quality criteria and candidate histological predictors.
    Leary AF; Castro DG; Nicholson AG; Ashley S; Wotherspoon A; O'Brien ME; Popat S
    Eur J Cancer; 2012 Jan; 48(1):61-7. PubMed ID: 22036089
    [TBL] [Abstract][Full Text] [Related]  

  • 16. EGFR testing and erlotinib use in non-small cell lung cancer patients in Kentucky.
    Larson KL; Huang B; Chen Q; Tucker T; Schuh M; Arnold SM; Kolesar JM
    PLoS One; 2020; 15(8):e0237790. PubMed ID: 32810185
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Type 2 Congenital Generalized Lipodystrophy: The Diagnosis is in Your Hands.
    Montenegro RM; Fernandes VO; Penaforte Saboia JG; Montenegro APDR; Lima JG
    J Pediatr; 2019 Apr; 207():257-257.e1. PubMed ID: 30579587
    [No Abstract]   [Full Text] [Related]  

  • 18. Simultaneous mutation scanning for gross deletions, duplications and point mutations in the DMD gene.
    Ashton EJ; Yau SC; Deans ZC; Abbs SJ
    Eur J Hum Genet; 2008 Jan; 16(1):53-61. PubMed ID: 17726484
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Uptake of prenatal diagnostic testing for retinoblastoma compared to other hereditary cancer syndromes in the Netherlands.
    Dommering CJ; Henneman L; van der Hout AH; Jonker MA; Tops CM; van den Ouweland AM; van der Luijt RB; Mensenkamp AR; Hogervorst FB; Redeker EJ; de Die-Smulders CE; Moll AC; Meijers-Heijboer H
    Fam Cancer; 2017 Apr; 16(2):271-277. PubMed ID: 27826806
    [TBL] [Abstract][Full Text] [Related]  

  • 20. EGFR mutation testing and TKI treatment patterns among veterans with stage III and IV non-small cell lung cancer.
    Hung A; Lee KM; Alba PR; Li Y; Gao AZ; Hintze BJ; Efimova OV; Shenolikar R; Pavilack M; Simmons D; Kelley MJ; Lynch JA; Reed SD
    Cancer Treat Res Commun; 2021; 27():100327. PubMed ID: 33549984
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.