BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

171 related articles for article (PubMed ID: 24898502)

  • 1. [Rare diseases are common].
    Has C; Giehl K
    Hautarzt; 2014 Jun; 65(6):488-9. PubMed ID: 24898502
    [No Abstract]   [Full Text] [Related]  

  • 2. [Genodermatoses with malignant skin tumors].
    Hübinger L; Frank J
    Hautarzt; 2014 Jun; 65(6):527-35. PubMed ID: 24898507
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A multistep approach to the diagnosis of rare genodermatoses.
    Tantcheva-Poór I; Oji V; Has C
    J Dtsch Dermatol Ges; 2016 Oct; 14(10):969-986. PubMed ID: 27767270
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [How frequently does genetic mosaicism occur in the skin?].
    Happle R
    Hautarzt; 2014 Jun; 65(6):536-41. PubMed ID: 24898508
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Alopecia and hypotrichosis in childhood: clinical features and diagnosis].
    Betz RC
    Hautarzt; 2014 Jun; 65(6):520-6. PubMed ID: 24898506
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Practical aspects of molecular diagnostics in genodermatoses].
    Has C; He Y
    Hautarzt; 2016 Jan; 67(1):53-8. PubMed ID: 26537890
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Vulvar Dyschromia in a Child: A Quiz.
    de Lorenzi C; Kaya G; Quenan S; Calza AM
    Acta Derm Venereol; 2019 Jun; 99(7):711-712. PubMed ID: 30938832
    [No Abstract]   [Full Text] [Related]  

  • 8. Generalized Skin Scaling in a Young Girl: A Quiz.
    Mo R; Wang H; Lin Z
    Acta Derm Venereol; 2019 Dec; 99(13):1322-1323. PubMed ID: 31612237
    [No Abstract]   [Full Text] [Related]  

  • 9. 23andMe resumes giving consumers genetic health information: Company's tests for rare and common diseases aren't diagnostic.
    Am J Med Genet A; 2017 Aug; 173(8):2003-2004. PubMed ID: 28703454
    [No Abstract]   [Full Text] [Related]  

  • 10. [Ophthalmogenetics: Rare Diseases - A Challenge for Diagnostic and Treatment].
    Rudolph G
    Klin Monbl Augenheilkd; 2016 Mar; 232(3):242. PubMed ID: 27011027
    [No Abstract]   [Full Text] [Related]  

  • 11. Adopting orphans: comprehensive genetic testing of Mendelian diseases of childhood by next-generation sequencing.
    Kingsmore SF; Dinwiddie DL; Miller NA; Soden SE; Saunders CJ
    Expert Rev Mol Diagn; 2011 Nov; 11(8):855-68. PubMed ID: 22022947
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Phen-Gen: combining phenotype and genotype to analyze rare disorders.
    Javed A; Agrawal S; Ng PC
    Nat Methods; 2014 Sep; 11(9):935-7. PubMed ID: 25086502
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Genodermatoses].
    Frank J
    Hautarzt; 2004 Oct; 55(10):919. PubMed ID: 15635734
    [No Abstract]   [Full Text] [Related]  

  • 14. Rare conditions: where do primary care and genetic diseases intersect?
    Terry SF; Krokosky A
    JAAPA; 2010 Nov; 23(11):63-4. PubMed ID: 21086896
    [No Abstract]   [Full Text] [Related]  

  • 15. Painful subcutaneous nodules in a patient with shortened digits.
    Johnson BC; Morrell DS
    Pediatr Dermatol; 2019 Nov; 36(6):944-945. PubMed ID: 31778566
    [No Abstract]   [Full Text] [Related]  

  • 16. Ligneous conjunctivitis in a young patient with homozygous K19E plasminogen gene mutation: a diagnostic and therapeutic challenge.
    Kuonen A; Vaudaux J; Hamedani M; Schuster V; Albisetti M; von der Weid N; Kaeser PF
    Klin Monbl Augenheilkd; 2013 Apr; 230(4):346-8. PubMed ID: 23629776
    [No Abstract]   [Full Text] [Related]  

  • 17. Next Generation Diagnostics for Rare Neurological Diseases: The Future is Here.
    Innes AM; Boycott KM
    Can J Neurol Sci; 2014 May; 41(3):299-300. PubMed ID: 24718813
    [No Abstract]   [Full Text] [Related]  

  • 18. Ending a Diagnostic Odyssey: Family Education, Counseling, and Response to Eventual Diagnosis.
    Basel D; McCarrier J
    Pediatr Clin North Am; 2017 Feb; 64(1):265-272. PubMed ID: 27894449
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A multistep approach to the diagnosis of rare genodermatoses.
    Aşkın Ö; Engin B; Gencebay G; Tüzün Y
    Clin Dermatol; 2020; 38(4):399-407. PubMed ID: 32972599
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The Molecular Revolution in Cutaneous Biology: Era of Molecular Diagnostics for Inherited Skin Diseases.
    McGrath JA
    J Invest Dermatol; 2017 May; 137(5):e83-e86. PubMed ID: 28411852
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.