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 *

88 related articles for article (PubMed ID: 1538745)

  • 1. Disease and development.
    Walter MA; Goodfellow PN
    Nature; 1992 Feb; 355(6361):590-1. PubMed ID: 1538745
    [No Abstract]   [Full Text] [Related]  

  • 2. Three novel PAX3 mutations observed in patients with Waardenburg syndrome type 1.
    Soejima H; Fujimoto M; Tsukamoto K; Matsumoto N; Yoshiura KI; Fukushima Y; Jinno Y; Niikawa N
    Hum Mutat; 1997; 9(2):177-80. PubMed ID: 9067759
    [No Abstract]   [Full Text] [Related]  

  • 3. PAX3 gene structure and mutations: close analogies between Waardenburg syndrome and the Splotch mouse.
    Tassabehji M; Newton VE; Leverton K; Turnbull K; Seemanova E; Kunze J; Sperling K; Strachan T; Read AP
    Hum Mol Genet; 1994 Jul; 3(7):1069-74. PubMed ID: 7981674
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Pax3 is required for enteric ganglia formation and functions with Sox10 to modulate expression of c-ret.
    Lang D; Chen F; Milewski R; Li J; Lu MM; Epstein JA
    J Clin Invest; 2000 Oct; 106(8):963-71. PubMed ID: 11032856
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A splice junction mutation in PAX3 causes Waardenburg syndrome in a South African family.
    Butt J; Greenberg J; Winship I; Sellars S; Beighton P; Ramesar R
    Hum Mol Genet; 1994 Jan; 3(1):197-8. PubMed ID: 8162027
    [No Abstract]   [Full Text] [Related]  

  • 6. Pax3 and vertebrate development.
    Epstein JA
    Methods Mol Biol; 2000; 137():459-70. PubMed ID: 10948560
    [No Abstract]   [Full Text] [Related]  

  • 7. [Clinical and molecular genetic investigation of Waardenburg syndrome type 1].
    Markova TG; Megrelishvilli SM; Shevtsov SP; Shvarts EI
    Vestn Otorinolaringol; 2003; (1):17-9. PubMed ID: 12666593
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Two different PAX3 gene mutations causing Waardenburg syndrome type I.
    Wildhardt G; Winterpacht A; Hilbert K; Menger H; Zabel B
    Mol Cell Probes; 1996 Jun; 10(3):229-31. PubMed ID: 8799378
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mutations in the PAX3 gene causing Waardenburg syndrome type 1 and type 2.
    Tassabehji M; Read AP; Newton VE; Patton M; Gruss P; Harris R; Strachan T
    Nat Genet; 1993 Jan; 3(1):26-30. PubMed ID: 8490648
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Myelomeningocele and Waardenburg syndrome (type 3) in patients with interstitial deletions of 2q35 and the PAX3 gene: possible digenic inheritance of a neural tube defect.
    Nye JS; Balkin N; Lucas H; Knepper PA; McLone DG; Charrow J
    Am J Med Genet; 1998 Feb; 75(4):401-8. PubMed ID: 9482647
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A splice-site mutation affecting the paired box of PAX3 in a three generation family with Waardenburg syndrome type I (WS1).
    Attaie A; Kim E; Wilcox ER; Lalwani AK
    Mol Cell Probes; 1997 Jun; 11(3):233-6. PubMed ID: 9232624
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Waardenburg's syndrome patients have mutations in the human homologue of the Pax-3 paired box gene.
    Tassabehji M; Read AP; Newton VE; Harris R; Balling R; Gruss P; Strachan T
    Nature; 1992 Feb; 355(6361):635-6. PubMed ID: 1347148
    [TBL] [Abstract][Full Text] [Related]  

  • 13. An exonic mutation in the HuP2 paired domain gene causes Waardenburg's syndrome.
    Baldwin CT; Hoth CF; Amos JA; da-Silva EO; Milunsky A
    Nature; 1992 Feb; 355(6361):637-8. PubMed ID: 1347149
    [TBL] [Abstract][Full Text] [Related]  

  • 14. X-linked albinism-deafness syndrome and Waardenburg syndrome type II: a hypothesis.
    Zlotogora J
    Am J Med Genet; 1995 Nov; 59(3):386-7. PubMed ID: 8599367
    [No Abstract]   [Full Text] [Related]  

  • 15. Chromosome 13q deletion with Waardenburg syndrome: further evidence for a gene involved in neural crest function on 13q.
    Van Camp G; Van Thienen MN; Handig I; Van Roy B; Rao VS; Milunsky A; Read AP; Baldwin CT; Farrer LA; Bonduelle M
    J Med Genet; 1995 Jul; 32(7):531-6. PubMed ID: 7562965
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Possible homozygous Waardenburg syndrome in a fetus with exencephaly.
    Aymé S; Philip N
    Am J Med Genet; 1995 Nov; 59(2):263-5. PubMed ID: 8588597
    [No Abstract]   [Full Text] [Related]  

  • 17. [Inner ear, sense of balance and the skull base]].
    Riemann R
    Laryngorhinootologie; 2004 Mar; 83(3):199. PubMed ID: 15088598
    [No Abstract]   [Full Text] [Related]  

  • 18. A plus-one frameshift mutation in PAX3 alters the entire deduced amino acid sequence of the paired box in a Waardenburg syndrome type 1 (WS1) family.
    Morell R; Friedman TB; Asher JH
    Hum Mol Genet; 1993 Sep; 2(9):1487-8. PubMed ID: 7902163
    [No Abstract]   [Full Text] [Related]  

  • 19. Mutations in PAX3 associated with Waardenburg syndrome type I.
    Baldwin CT; Lipsky NR; Hoth CF; Cohen T; Mamuya W; Milunsky A
    Hum Mutat; 1994; 3(3):205-11. PubMed ID: 8019556
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Analysis of locus heterogeneity in Waardenburg syndrome types 1 and 2 using highly informative microsatellite markers.
    Reynolds JE; Arnos KS; Landa B; Stevens CA; Salbert BA; Wright L; Duke B; Hunt W; Marazita ML; Ploughman L
    Hum Hered; 1995; 45(5):243-52. PubMed ID: 7590754
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.