120 related articles for article (PubMed ID: 7529555)
1. Localization of Beckwith-Wiedemann and rhabdoid tumor chromosome rearrangements to a defined interval in chromosome band 11p15.5.
Sait SN; Nowak NJ; Singh-Kahlon P; Weksberg R; Squire J; Shows TB; Higgins MJ
Genes Chromosomes Cancer; 1994 Oct; 11(2):97-105. PubMed ID: 7529555
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. 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]
5. A novel human homologue of yeast nucleosome assembly protein, 65 kb centromeric to the p57KIP2 gene, is biallelically expressed in fetal and adult tissues.
Hu RJ; Lee MP; Johnson LA; Feinberg AP
Hum Mol Genet; 1996 Nov; 5(11):1743-8. PubMed ID: 8923002
[TBL] [Abstract][Full Text] [Related]
6. 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; Voûte 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]
7. Chromosomal rearrangements in the 11p15 imprinted region: 17 new 11p15.5 duplications with associated phenotypes and putative functional consequences.
Heide S; Chantot-Bastaraud S; Keren B; Harbison MD; Azzi S; Rossignol S; Michot C; Lackmy-Port Lys M; Demeer B; Heinrichs C; Newfield RS; Sarda P; Van Maldergem L; Trifard V; Giabicani E; Siffroi JP; Le Bouc Y; Netchine I; Brioude F
J Med Genet; 2018 Mar; 55(3):205-213. PubMed ID: 29223973
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. 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]
11. Allelic methylation of H19 and IGF2 in the Beckwith-Wiedemann syndrome.
Reik W; Brown KW; Slatter RE; Sartori P; Elliott M; Maher ER
Hum Mol Genet; 1994 Aug; 3(8):1297-301. PubMed ID: 7987305
[TBL] [Abstract][Full Text] [Related]
12. A radiation hybrid map of the distal short arm of human chromosome 11, containing the Beckwith-Wiedemann and associated embryonal tumor disease loci.
Richard CW; Boehnke M; Berg DJ; Lichy JH; Meeker TC; Hauser E; Myers RM; Cox DR
Am J Hum Genet; 1993 May; 52(5):915-21. PubMed ID: 8387721
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. An integrated physical map of 210 markers assigned to the short arm of human chromosome 11.
Redeker E; Hoovers JM; Alders M; van Moorsel CJ; Ivens AC; Gregory S; Kalikin L; Bliek J; de Galan L; van den Bogaard R
Genomics; 1994 Jun; 21(3):538-50. PubMed ID: 7959730
[TBL] [Abstract][Full Text] [Related]
15. A 1-Mb physical map and PAC contig of the imprinted domain in 11p15.5 that contains TAPA1 and the BWSCR1/WT2 region.
Reid LH; Davies C; Cooper PR; Crider-Miller SJ; Sait SN; Nowak NJ; Evans G; Stanbridge EJ; deJong P; Shows TB; Weissman BE; Higgins MJ
Genomics; 1997 Aug; 43(3):366-75. PubMed ID: 9268640
[TBL] [Abstract][Full Text] [Related]
16. A fine-structure deletion map of human chromosome 11p: analysis of J1 series hybrids.
Glaser T; Housman D; Lewis WH; Gerhard D; Jones C
Somat Cell Mol Genet; 1989 Nov; 15(6):477-501. PubMed ID: 2595451
[TBL] [Abstract][Full Text] [Related]
17. Fibroadenoma in Beckwith-Wiedemann syndrome with paternal uniparental disomy of chromosome 11p15.5.
Takama Y; Kubota A; Nakayama M; Higashimoto K; Jozaki K; Soejima H
Pediatr Int; 2014 Dec; 56(6):931-934. PubMed ID: 25521982
[TBL] [Abstract][Full Text] [Related]
18. Molecular biology of Beckwith-Wiedemann syndrome.
Weksberg R; Squire JA
Med Pediatr Oncol; 1996 Nov; 27(5):462-9. PubMed ID: 8827075
[TBL] [Abstract][Full Text] [Related]
19. Targeted disruption of the human LIT1 locus defines a putative imprinting control element playing an essential role in Beckwith-Wiedemann syndrome.
Horike S; Mitsuya K; Meguro M; Kotobuki N; Kashiwagi A; Notsu T; Schulz TC; Shirayoshi Y; Oshimura M
Hum Mol Genet; 2000 Sep; 9(14):2075-83. PubMed ID: 10958646
[TBL] [Abstract][Full Text] [Related]
20. Alterations of H19 imprinting and IGF2 replication timing are infrequent in Beckwith-Wiedemann syndrome.
Squire JA; Li M; Perlikowski S; Fei YL; Bayani J; Zhang ZM; Weksberg R
Genomics; 2000 May; 65(3):234-42. PubMed ID: 10857747
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
