BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

162 related articles for article (PubMed ID: 2921038)

  • 1. Molecular definition of the 11p15.5 region involved in Beckwith-Wiedemann syndrome and probably in predisposition to adrenocortical carcinoma.
    Henry I; Jeanpierre M; Couillin P; Barichard F; Serre JL; Journel H; Lamouroux A; Turleau C; de Grouchy J; Junien C
    Hum Genet; 1989 Feb; 81(3):273-7. PubMed ID: 2921038
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Molecular characterization of cytogenetic alterations associated with the Beckwith-Wiedemann syndrome (BWS) phenotype refines the localization and suggests the gene for BWS is imprinted.
    Weksberg R; Teshima I; Williams BR; Greenberg CR; Pueschel SM; Chernos JE; Fowlow SB; Hoyme E; Anderson IJ; Whiteman DA
    Hum Mol Genet; 1993 May; 2(5):549-56. PubMed ID: 8518793
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Molecular and genomic characterisation of cryptic chromosomal alterations leading to paternal duplication of the 11p15.5 Beckwith-Wiedemann region.
    Russo S; Finelli P; Recalcati MP; Ferraiuolo S; Cogliati F; Dalla Bernardina B; Tibiletti MG; Agosti M; Sala M; Bonati MT; Larizza L
    J Med Genet; 2006 Aug; 43(8):e39. PubMed ID: 16882733
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A new case of Beckwith-Wiedemann syndrome with an 11p15 duplication of paternal origin [46,XY,-21,+der(21), t(11;21)(p15.2;q22.3)pat].
    Krajewska-Walasek M; Gutkowska A; Mospinek-Krasnopolska M; Chrzanowska K
    Acta Genet Med Gemellol (Roma); 1996; 45(1-2):245-50. PubMed ID: 8872040
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Paternally inherited duplications of 11p15.5 and Beckwith-Wiedemann syndrome.
    Slavotinek A; Gaunt L; Donnai D
    J Med Genet; 1997 Oct; 34(10):819-26. PubMed ID: 9350814
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Beckwith-Wiedemann syndrome due to 11p15.5 paternal duplication associated with Klinefelter syndrome and a "de novo" pericentric inversion of chromosome Y.
    Delicado A; Lapunzina P; Palomares M; Molina MA; Galán E; López Pajares I
    Eur J Med Genet; 2005; 48(2):159-66. PubMed ID: 16053907
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Paternal origin of 11p15 duplications in the Beckwith-Wiedemann syndrome. A new case and review of the literature.
    Brown KW; Gardner A; Williams JC; Mott MG; McDermott A; Maitland NJ
    Cancer Genet Cytogenet; 1992 Jan; 58(1):66-70. PubMed ID: 1728953
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Unbalanced segregation of a paternal t(9;11)(p24.3;p15.4) translocation causing familial Beckwith-Wiedemann syndrome: a case report.
    Lekszas C; Nanda I; Vona B; Böck J; Ashrafzadeh F; Donyadideh N; Ebrahimzadeh F; Ahangari N; Maroofian R; Karimiani EG; Haaf T
    BMC Med Genomics; 2019 Jun; 12(1):83. PubMed ID: 31174542
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A constitutional BWS-related t(11;16) chromosome translocation occurring in the same region of chromosome 16 implicated in Wilms' tumors.
    Newsham I; Kindler-Röhrborn A; Daub D; Cavenee W
    Genes Chromosomes Cancer; 1995 Jan; 12(1):1-7. PubMed ID: 7534105
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Multiple genetic loci within 11p15 defined by Beckwith-Wiedemann syndrome rearrangement breakpoints and subchromosomal transferable fragments.
    Hoovers JM; Kalikin LM; Johnson LA; Alders M; Redeker B; Law DJ; Bliek J; Steenman M; Benedict M; Wiegant J; Lengauer C; Taillon-Miller P; Schlessinger D; Edwards MC; Elledge SJ; Ivens A; Westerveld A; Little P; Mannens M; Feinberg AP
    Proc Natl Acad Sci U S A; 1995 Dec; 92(26):12456-60. PubMed ID: 8618920
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Sex dependent transmission of Beckwith-Wiedemann syndrome associated with a reciprocal translocation t(9;11)(p11.2;p15.5).
    Tommerup N; Brandt CA; Pedersen S; Bolund L; Kamper J
    J Med Genet; 1993 Nov; 30(11):958-61. PubMed ID: 8301654
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Molecular characterization of Beckwith-Wiedemann syndrome (BWS) patients with partial duplication of chromosome 11p excludes the gene MYOD1 from the BWS region.
    Weksberg R; Glaves M; Teshima I; Waziri M; Patil S; Williams BR
    Genomics; 1990 Dec; 8(4):693-8. PubMed ID: 2276740
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Tumor-specific loss of 11p15.5 alleles in del11p13 Wilms tumor and in familial adrenocortical carcinoma.
    Henry I; Grandjouan S; Couillin P; Barichard F; Huerre-Jeanpierre C; Glaser T; Philip T; Lenoir G; Chaussain JL; Junien C
    Proc Natl Acad Sci U S A; 1989 May; 86(9):3247-51. PubMed ID: 2566168
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Parental imprinting of human chromosome region 11p15.3-pter involved in the Beckwith-Wiedemann syndrome and various human neoplasia.
    Mannens M; Hoovers JM; Redeker E; Verjaal M; Feinberg AP; Little P; Boavida M; Coad N; Steenman M; Bliek J
    Eur J Hum Genet; 1994; 2(1):3-23. PubMed ID: 7913866
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 11p15.5-specific libraries for identification of potential gene sequences involved in Beckwith-Wiedemann syndrome and tumorigenesis.
    Puech A; Ahnine L; Lüdecke HJ; Senger G; Ivens A; Jeanpierre C; Little P; Horsthemke B; Claussen U; Jones C
    Genomics; 1992 Aug; 13(4):1274-80. PubMed ID: 1380484
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Familial Wiedemann-Beckwith syndrome and a second Wilms tumor locus both map to 11p15.5.
    Koufos A; Grundy P; Morgan K; Aleck KA; Hadro T; Lampkin BC; Kalbakji A; Cavenee WK
    Am J Hum Genet; 1989 May; 44(5):711-9. PubMed ID: 2539717
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Beckwith-Wiedemann syndrome and long QT syndrome due to familial-balanced translocation t(11;17)(p15.5;q21.3) involving the KCNQ1 gene.
    Kaltenbach S; Capri Y; Rossignol S; Denjoy I; Soudée S; Aboura A; Baumann C; Verloes A
    Clin Genet; 2013 Jul; 84(1):78-81. PubMed ID: 23061425
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genetic linkage of Beckwith-Wiedemann syndrome to 11p15.
    Ping AJ; Reeve AE; Law DJ; Young MR; Boehnke M; Feinberg AP
    Am J Hum Genet; 1989 May; 44(5):720-3. PubMed ID: 2565083
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Loss of alleles on the short arm of chromosome 11 in a hepatoblastoma from a child with Beckwith-Wiedemann syndrome.
    Little MH; Thomson DB; Hayward NK; Smith PJ
    Hum Genet; 1988 Jun; 79(2):186-9. PubMed ID: 2839410
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Characterization of the breakpoints in unbalanced t(5;11)(p15;p15) constitutional chromosome translocations in two patients with beckwith-wiedemann syndrome using fluorescence in situ hybridisation.
    Grundy RG; Aledo R; Cowell JK
    Int J Mol Med; 1998 May; 1(5):801-8. PubMed ID: 9852299
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.