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 *

115 related articles for article (PubMed ID: 10191630)

  • 1. [Molecular-genetic approach to congenital malformation syndromes].
    Niikawa N
    No To Hattatsu; 1999 Mar; 31(2):105-13. PubMed ID: 10191630
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Positional cloning of genes involved in the Beckwith-Wiedemann syndrome, hemihypertrophy, and associated childhood tumors.
    Mannens M; Alders M; Redeker B; Bliek J; Steenman M; Wiesmeyer C; de Meulemeester M; Ryan A; Kalikin L; Voƻte T; De Kraker J; Hoovers J; Slater R; Feinberg A; Little P; Westerveld A
    Med Pediatr Oncol; 1996 Nov; 27(5):490-4. PubMed ID: 8827079
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Current status of the human malformation map.
    Carey JC; Viskochil DH
    Birth Defects Orig Artic Ser; 1996; 30(1):13-34. PubMed ID: 9125323
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Current advances in the cytogenetics and molecular biology of the diagnosis of malformation syndromes].
    Dallapiccola B; Mingarelli R; Zelante L
    Pediatr Med Chir; 1993; 15 Suppl 1():10-3. PubMed ID: 8415186
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Seven megabase yeast artificial chromosome contig at region 11p15: identification of a yeast artificial chromosome spanning the breakpoint of a chromosomal translocation found in a case of Beckwith-Wiedemann syndrome.
    Negrini M; Sabbioni S; Ohta M; Veronese ML; Rattan S; Junien C; Croce CM
    Cancer Res; 1995 Jul; 55(13):2904-9. PubMed ID: 7796419
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Physical mapping of 3 candidate tumor suppressor genes relative to Beckwith-Wiedemann syndrome associated chromosomal breakpoints at 11p15.3.
    Redeker E; Alders M; Hoovers JM; Richard CW; Westerveld A; Mannens M
    Cytogenet Cell Genet; 1995; 68(3-4):222-5. PubMed ID: 7842740
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Teaching molecular genetics: chapter 4-positional cloning of genetic disorders.
    Puliti A; Caridi G; Ravazzolo R; Ghiggeri GM
    Pediatr Nephrol; 2007 Dec; 22(12):2023-9. PubMed ID: 17661092
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [The Wiedemann-Beckwith syndrome and a congenital cataract].
    Momtchilova M; Pelosse B; Laroche L; Vazquez MP
    J Fr Ophtalmol; 2001 May; 24(5):479-81. PubMed ID: 11397983
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Tracking disease genes by reverse genetics.
    Pignatti PF; Turco AE
    J Psychiatr Res; 1992 Oct; 26(4):287-98. PubMed ID: 1491355
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Waardenburg syndrome in man and splotch mutants in the mouse: a paradigm of the usefulness of linkage and synteny homologies in mouse and man for the genetic analysis of human congenital malformations.
    Delezoide AL; Vekemans M
    Biomed Pharmacother; 1994; 48(8-9):335-9. PubMed ID: 7858167
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Human KVLQT1 gene shows tissue-specific imprinting and encompasses Beckwith-Wiedemann syndrome chromosomal rearrangements.
    Lee MP; Hu RJ; Johnson LA; Feinberg AP
    Nat Genet; 1997 Feb; 15(2):181-5. PubMed ID: 9020845
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Malformation syndromes: a review of mouse/human homology.
    Winter RM
    J Med Genet; 1988 Jul; 25(7):480-7. PubMed ID: 3050095
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Molecular genetics of inherited chorioretinal dystrophy--strategy for identifying disease causing genes].
    Mashima Y
    Nippon Ganka Gakkai Zasshi; 1999 Mar; 103(3):165-77. PubMed ID: 10214050
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Positional cloning moves from perditional to traditional.
    Collins FS
    Nat Genet; 1995 Apr; 9(4):347-50. PubMed ID: 7795639
    [TBL] [Abstract][Full Text] [Related]  

  • 15. From linked marker to gene.
    Wicking C; Williamson B
    Trends Genet; 1991 Sep; 7(9):288-93. PubMed ID: 1763426
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Cloning of candidate genes involved in the Beckwith-Wiedemann syndrome and childhood tumors.
    Alders M; Bliek J; Redeker B; Ryan A; Feinberg A; Westerveld A; Little P; Mannens M
    Med Pediatr Oncol; 1996 Nov; 27(5):495-7. PubMed ID: 8827080
    [No Abstract]   [Full Text] [Related]  

  • 17. p57KIP2 targeted disruption and Beckwith-Wiedemann syndrome: is the inhibitor just a contributor?
    Swanger WJ; Roberts JM
    Bioessays; 1997 Oct; 19(10):839-42. PubMed ID: 9363677
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The zon laboratory guide to positional cloning in zebrafish.
    Zhou Y; Zon LI
    Methods Cell Biol; 2011; 104():287-309. PubMed ID: 21924169
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Fluorescence in situ hybridization mapping of 25 markers on distal human chromosome 2q surrounding the human Waardenburg syndrome, type I (WS1) locus (PAX3 gene).
    Lu-Kuo J; Ward DC; Spritz RA
    Genomics; 1993 Apr; 16(1):173-9. PubMed ID: 8486353
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Basic elements of gene mapping and identification.
    Consevage M; Cyran S
    Curr Opin Cardiol; 1997 May; 12(3):288-94. PubMed ID: 9243086
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.