161 related articles for article (PubMed ID: 31254405)
1. Clinical genetic testing in endocrinology: Current concepts and contemporary challenges.
Newey PJ
Clin Endocrinol (Oxf); 2019 Nov; 91(5):587-607. PubMed ID: 31254405
[TBL] [Abstract][Full Text] [Related]
2. A practical guide to genetic testing in endocrinology.
Izatt L; Owens MM; Pierce H; Wilcox S; Park SM
Clin Endocrinol (Oxf); 2022 Oct; 97(4):388-399. PubMed ID: 34528717
[TBL] [Abstract][Full Text] [Related]
3. Molecular genetic testing in endocrinology - a practical guide.
Kirmani S
Endocr Pract; 2012; 18(1):85-9. PubMed ID: 22336444
[TBL] [Abstract][Full Text] [Related]
4. Search for Novel Mutational Targets in Human Endocrine Diseases.
Park SY; Seo MH; Lee S
Endocrinol Metab (Seoul); 2019 Mar; 34(1):23-28. PubMed ID: 30912335
[TBL] [Abstract][Full Text] [Related]
5. Next generation sequencing in endocrine practice.
Forlenza GP; Calhoun A; Beckman KB; Halvorsen T; Hamdoun E; Zierhut H; Sarafoglou K; Polgreen LE; Miller BS; Nathan B; Petryk A
Mol Genet Metab; 2015; 115(2-3):61-71. PubMed ID: 25958132
[TBL] [Abstract][Full Text] [Related]
6. Applications of molecular biology and genetics in endocrinology.
Kopp P
Endocr Pract; 2007 Sep; 13(5):534-41. PubMed ID: 17872356
[TBL] [Abstract][Full Text] [Related]
7. Next generation sequencing for disorders of sex development.
Tobias ES; McElreavey K
Endocr Dev; 2014; 27():53-62. PubMed ID: 25247644
[TBL] [Abstract][Full Text] [Related]
8. NGS-Based genetic testing for heritable cardiovascular diseases. Specific requirements for obtaining informed consent.
Schmidtke J; Wittkowski K; Glaubitz R
Mol Cell Probes; 2019 Jun; 45():70-78. PubMed ID: 31059777
[TBL] [Abstract][Full Text] [Related]
9. Challenges to clinical utilization of hereditary cancer gene panel testing: perspectives from the front lines.
Marcus RK; Geurts JL; Grzybowski JA; Turaga KK; Clark Gamblin T; Strong KA; Johnston FM
Fam Cancer; 2015 Dec; 14(4):641-9. PubMed ID: 26108897
[TBL] [Abstract][Full Text] [Related]
10. Next generation sequencing in hematolymphoid neoplasia.
Kuo FC
Semin Hematol; 2019 Jan; 56(1):2-6. PubMed ID: 30573040
[TBL] [Abstract][Full Text] [Related]
11. [Molecular tests for (early) recognition of endocrine disorders - towards a sophisticated management of complex endocrine and metabolic diseases].
Kopp P
Ther Umsch; 2010 Jul; 67(7):367-73. PubMed ID: 20577965
[TBL] [Abstract][Full Text] [Related]
12. Genetic testing in inherited endocrine disorders: joint position paper of the European reference network on rare endocrine conditions (Endo-ERN).
Eggermann T; Elbracht M; Kurth I; Juul A; Johannsen TH; Netchine I; Mastorakos G; Johannsson G; Musholt TJ; Zenker M; Prawitt D; Pereira AM; Hiort O;
Orphanet J Rare Dis; 2020 Jun; 15(1):144. PubMed ID: 32513286
[TBL] [Abstract][Full Text] [Related]
13. Molecular genetic testing strategies used in diagnostic flow for hereditary endocrine tumour syndromes.
Butz H; Blair J; Patócs A
Endocrine; 2021 Mar; 71(3):641-652. PubMed ID: 33570725
[TBL] [Abstract][Full Text] [Related]
14. GENETICS IN ENDOCRINOLOGY: Genetic diagnosis of endocrine diseases by NGS: novel scenarios and unpredictable results and risks.
Persani L; de Filippis T; Colombo C; Gentilini D
Eur J Endocrinol; 2018 Sep; 179(3):R111-R123. PubMed ID: 29880707
[TBL] [Abstract][Full Text] [Related]
15. Lessons learned: next-generation sequencing applied to undiagnosed genetic diseases.
Schuler BA; Nelson ET; Koziura M; Cogan JD; Hamid R; Phillips JA
J Clin Invest; 2022 Apr; 132(7):. PubMed ID: 35362483
[TBL] [Abstract][Full Text] [Related]
16. College of American Pathologists' laboratory standards for next-generation sequencing clinical tests.
Aziz N; Zhao Q; Bry L; Driscoll DK; Funke B; Gibson JS; Grody WW; Hegde MR; Hoeltge GA; Leonard DG; Merker JD; Nagarajan R; Palicki LA; Robetorye RS; Schrijver I; Weck KE; Voelkerding KV
Arch Pathol Lab Med; 2015 Apr; 139(4):481-93. PubMed ID: 25152313
[TBL] [Abstract][Full Text] [Related]
17. Genetic Testing in Endocrinology.
De Sousa SM; Hardy TS; Scott HS; Torpy DJ
Clin Biochem Rev; 2018 Feb; 39(1):17-28. PubMed ID: 30072819
[TBL] [Abstract][Full Text] [Related]
18. Evaluation of copy number variant detection from panel-based next-generation sequencing data.
Yao R; Yu T; Qing Y; Wang J; Shen Y
Mol Genet Genomic Med; 2019 Jan; 7(1):e00513. PubMed ID: 30565893
[TBL] [Abstract][Full Text] [Related]
19. A scoping study to explore the cost-effectiveness of next-generation sequencing compared with traditional genetic testing for the diagnosis of learning disabilities in children.
Beale S; Sanderson D; Sanniti A; Dundar Y; Boland A
Health Technol Assess; 2015 Jun; 19(46):1-90. PubMed ID: 26132578
[TBL] [Abstract][Full Text] [Related]
20. Maternal Plasma DNA and RNA Sequencing for Prenatal Testing.
Tamminga S; van Maarle M; Henneman L; Oudejans CB; Cornel MC; Sistermans EA
Adv Clin Chem; 2016; 74():63-102. PubMed ID: 27117661
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
