BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

206 related articles for article (PubMed ID: 12893942)

  • 41. Diaphragmatic hernia as the first echographic sign in Apert syndrome.
    Witters I; Devriendt K; Moerman P; van Hole C; Fryns JP
    Prenat Diagn; 2000 May; 20(5):404-6. PubMed ID: 10820409
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Trp290Cys mutation of the FGFR2 gene in a patient with severe Pfeiffer syndrome type 2.
    Ariga H; Endo Y; Ujiie N; Ishii T; Ishibashi N; Fujita T; Suzuki H
    Pediatr Int; 2001 Jun; 43(3):293-5. PubMed ID: 11380927
    [No Abstract]   [Full Text] [Related]  

  • 43. Epidermal mosaicism producing localised acne: somatic mutation in FGFR2.
    Munro CS; Wilkie AO
    Lancet; 1998 Aug; 352(9129):704-5. PubMed ID: 9728990
    [No Abstract]   [Full Text] [Related]  

  • 44. Mutation of FGFR2 (cys278phe) in craniolacunia and pansynostosis.
    Steinberger D; Müller U; Jünger TH; Howaldt HP; Christophis P
    J Med Genet; 1999 Jun; 36(6):499-500. PubMed ID: 10874645
    [No Abstract]   [Full Text] [Related]  

  • 45. The paternal-age effect in Apert syndrome is due, in part, to the increased frequency of mutations in sperm.
    Glaser RL; Broman KW; Schulman RL; Eskenazi B; Wyrobek AJ; Jabs EW
    Am J Hum Genet; 2003 Oct; 73(4):939-47. PubMed ID: 12900791
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Three craniosynostotic patients with tracheal sleeve.
    Okajima K; Aoki I; Sagehashi N; Malcolm S; Winter RM
    Clin Dysmorphol; 2003 Jan; 12(1):75. PubMed ID: 12514372
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Single nucleotide polymorphisms of the fibroblast growth factor receptor 2 gene in patients with chronic venous insufficiency with leg ulcer.
    Nagy N; Szolnoky G; Szabad G; Bata-Csörgo Z; Dobozy A; Kemeny L; Szell M
    J Invest Dermatol; 2005 May; 124(5):1085-8. PubMed ID: 15854058
    [No Abstract]   [Full Text] [Related]  

  • 48. A novel heterozygous mutation in FGFR2 gene causing Pfeiffer syndrome.
    Machado RA; Ferreira SB; Martins L; Ribeiro MM; Martelli DRB; Coletta RD; Aguiar MJB; Martelli-Júnior H
    Am J Med Genet A; 2017 Oct; 173(10):2838-2843. PubMed ID: 28815901
    [No Abstract]   [Full Text] [Related]  

  • 49. The observed human sperm mutation frequency cannot explain the achondroplasia paternal age effect.
    Tiemann-Boege I; Navidi W; Grewal R; Cohn D; Eskenazi B; Wyrobek AJ; Arnheim N
    Proc Natl Acad Sci U S A; 2002 Nov; 99(23):14952-7. PubMed ID: 12397172
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Age-Dependent De Novo Mutations During Spermatogenesis and Their Consequences.
    Cioppi F; Casamonti E; Krausz C
    Adv Exp Med Biol; 2019; 1166():29-46. PubMed ID: 31301044
    [TBL] [Abstract][Full Text] [Related]  

  • 51. New evidence for positive selection helps explain the paternal age effect observed in achondroplasia.
    Shinde DN; Elmer DP; Calabrese P; Boulanger J; Arnheim N; Tiemann-Boege I
    Hum Mol Genet; 2013 Oct; 22(20):4117-26. PubMed ID: 23740942
    [TBL] [Abstract][Full Text] [Related]  

  • 52. The molecular anatomy of spontaneous germline mutations in human testes.
    Qin J; Calabrese P; Tiemann-Boege I; Shinde DN; Yoon SR; Gelfand D; Bauer K; Arnheim N
    PLoS Biol; 2007 Sep; 5(9):e224. PubMed ID: 17760502
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Age and sex effects on human mutation rates: an old problem with new complexities.
    Crow JF
    J Radiat Res; 2006; 47 Suppl B():B75-82. PubMed ID: 17019055
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Selective mutation accumulation: a computational model of the paternal age effect.
    Whelan EC; Nwala AC; Osgood C; Olariu S
    Bioinformatics; 2016 Dec; 32(24):3790-3797. PubMed ID: 27531106
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Hunterian Lecture. What can we learn about mechanisms of mutation from a study of craniosynostosis?
    Moloney D
    Ann R Coll Surg Engl; 2001 Jan; 83(1):1-9. PubMed ID: 11212439
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Upsetting the dogma: germline selection in human males.
    Crow JF
    PLoS Genet; 2012; 8(2):e1002535. PubMed ID: 22359519
    [No Abstract]   [Full Text] [Related]  

  • 57. Too old to be a dad?
    Kluger J; Birmingham L; Koningsberg RD; Park A; Thean T; Cabrera F; Mahr K
    Time; 2013 Apr; 181(15):38-43. PubMed ID: 23898733
    [No Abstract]   [Full Text] [Related]  

  • 58. Missing heritability: paternal age effect mutations and selfish spermatogonia.
    Goriely A; Wilkie AO
    Nat Rev Genet; 2010 Aug; 11(8):589. PubMed ID: 20634812
    [No Abstract]   [Full Text] [Related]  

  • 59. Paternal age effect mutations and selfish spermatogonial selection: causes and consequences for human disease.
    Goriely A; Wilkie AO
    Am J Hum Genet; 2012 Feb; 90(2):175-200. PubMed ID: 22325359
    [TBL] [Abstract][Full Text] [Related]  

  • 60.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.