174 related articles for article (PubMed ID: 2176177)
21. Acrocentric chromosome polymorphisms: beware of cryptic translocations.
Benzacken B; Monier-Gavelle F; Siffroi JP; Agbo P; Chalvon A; Wolf JP
Prenat Diagn; 2001 Feb; 21(2):96-8. PubMed ID: 11241533
[TBL] [Abstract][Full Text] [Related]
22. Single cell analysis demonstrating somatic mosaicism involving 11p in a patient with paternal isodisomy and Beckwith-Wiedemann syndrome.
Bischoff FZ; Feldman GL; McCaskill C; Subramanian S; Hughes MR; Shaffer LG
Hum Mol Genet; 1995 Mar; 4(3):395-9. PubMed ID: 7795593
[TBL] [Abstract][Full Text] [Related]
23. Chromosomal assignment of six muscle-specific genes in cattle.
Ryan AM; Schelling CP; Womack JE; Gallagher DS
Anim Genet; 1997 Apr; 28(2):84-7. PubMed ID: 9172305
[TBL] [Abstract][Full Text] [Related]
24. Molecular analysis of patients with Wiedemann-Beckwith syndrome. I. Gene dosage on the short arm of chromosome 11.
Nyström A; Engström W; Cheetham J; Schofield PN
Eur J Pediatr; 1992 Jul; 151(7):504-10. PubMed ID: 1356784
[TBL] [Abstract][Full Text] [Related]
25. Cloning, expression and localization of human BM88 shows that it maps to chromosome 11p15.5, a region implicated in Beckwith-Wiedemann syndrome and tumorigenesis.
Gaitanou M; Buanne P; Pappa C; Georgopoulou N; Mamalaki A; Tirone F; Matsas R
Biochem J; 2001 May; 355(Pt 3):715-24. PubMed ID: 11311134
[TBL] [Abstract][Full Text] [Related]
26. 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]
27. Reassessment of breakpoints in chromosome 11p15.
Henry I; van Heyningen V; Puech A; Scrable H; Augereau P; Boehm T; Rabbitts T; Mannens M; Rochefort H; Jones C
Cytogenet Cell Genet; 1993; 62(1):52-3. PubMed ID: 8422757
[TBL] [Abstract][Full Text] [Related]
28. C11orf21, a novel gene within the Beckwith-Wiedemann syndrome region in human chromosome 11p15.5.
Zhu X; Higashimoto K; Soejima H; Yatsuki H; Sugihara H; Mukai T; Joh K
Gene; 2000 Oct; 256(1-2):311-7. PubMed ID: 11054561
[TBL] [Abstract][Full Text] [Related]
29. Generation of homozygosity at the c-Ha-ras-1 locus on chromosome 11p in an adrenal adenoma from an adult with Wiedemann-Beckwith syndrome.
Hayward NK; Little MH; Mortimer RH; Clouston WM; Smith PJ
Cancer Genet Cytogenet; 1988 Jan; 30(1):127-32. PubMed ID: 3275489
[TBL] [Abstract][Full Text] [Related]
30. Analysis of WAGR deletions and related translocations with gene-specific DNA probes, using FACS-selected cell hybrids.
Seawright A; Fletcher JM; Fantes JA; Morrison H; Porteous DJ; Li SS; Hastie ND; Van Heyningen V
Somat Cell Mol Genet; 1988 Jan; 14(1):21-30. PubMed ID: 2829363
[TBL] [Abstract][Full Text] [Related]
31. 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]
32. 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]
33. 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]
34. The human tyrosine aminotransferase gene mapped to the long arm of chromosome 16 (region 16q22----q24) by somatic cell hybrid analysis and in situ hybridization.
Barton DE; Yang-Feng TL; Francke U
Hum Genet; 1986 Mar; 72(3):221-4. PubMed ID: 2870017
[TBL] [Abstract][Full Text] [Related]
35. Wiedemann-Beckwith syndrome and chromosomal duplication 4q/deficiency 18p.
Fryns JP; Kleczkowska A; Devriendt K; Devliegher H; Van den Berghe H
Genet Couns; 1993; 4(1):37-41. PubMed ID: 8471219
[TBL] [Abstract][Full Text] [Related]
36. Trisomy 11p15 and Beckwith-Wiedemann syndrome. Report of two new cases.
Journel H; Lucas J; Allaire C; Le Mée F; Defawe G; Lecornu M; Jouan H; Roussey M; Le Marec B
Ann Genet; 1985; 28(2):97-101. PubMed ID: 3876070
[TBL] [Abstract][Full Text] [Related]
37. 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]
38. 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]
39. Human FRAG1 encodes a novel membrane-spanning protein that localizes to chromosome 11p15.5, a region of frequent loss of heterozygosity in cancer.
Lorenzi MV; Castagnino P; Aaronson DC; Lieb DC; Lee CC; Keck CL; Popescu NC; Miki T
Genomics; 1999 Nov; 62(1):59-66. PubMed ID: 10585768
[TBL] [Abstract][Full Text] [Related]
40. Microarray detection of a de novo der(X)t(X;11)(q28;p13) in a girl with premature ovarian failure and features of Beckwith-Wiedemann syndrome.
Han JY; Shin JH; Han MS; Je GH; Shaffer LG
J Hum Genet; 2006; 51(7):641-3. PubMed ID: 16708166
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]