182 related articles for article (PubMed ID: 2722195)
21. A highly polymorphic locus cloned from the breakpoint of a chromosome 11p13 deletion associated with the WAGR syndrome.
Glaser T; Driscoll DJ; Antonarakis S; Valle D; Housman D
Genomics; 1989 Nov; 5(4):880-93. PubMed ID: 2574149
[TBL] [Abstract][Full Text] [Related]
22. A common region of loss of heterozygosity in Wilms' tumor and embryonal rhabdomyosarcoma distal to the D11S988 locus on chromosome 11p15.5.
Besnard-Guérin C; Newsham I; Winqvist R; Cavenee WK
Hum Genet; 1996 Feb; 97(2):163-70. PubMed ID: 8566947
[TBL] [Abstract][Full Text] [Related]
23. Sequences which flank an 11p deletion observed in an hepatocellular carcinoma map to 11p13.
Fisher JH; Scoggin CH; Rogler CE
Hum Genet; 1987 Jan; 75(1):66-9. PubMed ID: 3026949
[TBL] [Abstract][Full Text] [Related]
24. Constitutional and somatic deletions of two different regions of maternal chromosome 11 in Wilms tumor.
Jeanpierre C; Antignac C; Beroud C; Lavedan C; Henry I; Saunders G; Williams B; Glaser T; Junien C
Genomics; 1990 Jul; 7(3):434-8. PubMed ID: 1973142
[TBL] [Abstract][Full Text] [Related]
25. CpG islands surround a DNA segment located between translocation breakpoints associated with genitourinary dysplasia and aniridia.
Bickmore WA; Porteous DJ; Christie S; Seawright A; Fletcher JM; Maule JC; Couillin P; Junien C; Hastie ND; van Heyningen V
Genomics; 1989 Nov; 5(4):685-93. PubMed ID: 2556343
[TBL] [Abstract][Full Text] [Related]
26. 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]
27. 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]
28. Microdissection of chromosome band 11p15.5: characterization of probes mapping distal to the HBBC locus.
Newsham I; Claussen U; Lüdecke HJ; Mason M; Senger G; Horsthemke B; Cavenee W
Genes Chromosomes Cancer; 1991 Mar; 3(2):108-16. PubMed ID: 1676905
[TBL] [Abstract][Full Text] [Related]
29. Deletion of WT1 and WIT1 genes and loss of heterozygosity on chromosome 11p in Wilms tumors in Japan.
Kaneko Y; Takeda O; Homma C; Maseki N; Miyoshi H; Tsunematsu Y; Williams BG; Saunders GF; Sakurai M
Jpn J Cancer Res; 1993 Jun; 84(6):616-24. PubMed ID: 8393432
[TBL] [Abstract][Full Text] [Related]
30. The chromosome 11 region flanking the t(11;14) breakpoint in human T-ALL is deleted in Wilms' tumor hybrids.
Finver SN; Martiniere C; Kagan J; Cavenee W; Croce CM
Oncogene Res; 1989; 5(2):143-8. PubMed ID: 2558334
[TBL] [Abstract][Full Text] [Related]
31. 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]
32. The T-ALL specific t(11;14)(p13;q11) translocation breakpoint cluster region is located near to the Wilms' tumour predisposition locus.
Boehm T; Lavenir I; Forster A; Wadey RB; Cowell JK; Harbott J; Lampert F; Waters J; Sherrington P; Couillin P
Oncogene; 1988 Dec; 3(6):691-5. PubMed ID: 2577871
[TBL] [Abstract][Full Text] [Related]
33. Four new DNA markers are assigned to the WAGR region of 11p13: isolation and regional assignment of 112 chromosome 11 anonymous DNA segments.
Davis LM; Byers MG; Fukushima Y; Qin SZ; Nowak NJ; Scoggin C; Shows TB
Genomics; 1988 Oct; 3(3):264-71. PubMed ID: 2852164
[TBL] [Abstract][Full Text] [Related]
34. Two anonymous DNA segments distinguish the Wilms' tumor and aniridia loci.
Davis LM; Stallard R; Thomas GH; Couillin P; Junien C; Nowak NJ; Shows TB
Science; 1988 Aug; 241(4867):840-2. PubMed ID: 2841760
[TBL] [Abstract][Full Text] [Related]
35. The recombination activating genes, RAG 1 and RAG 2, are on chromosome 11p in humans and chromosome 2p in mice.
Oettinger MA; Stanger B; Schatz DG; Glaser T; Call K; Housman D; Baltimore D
Immunogenetics; 1992; 35(2):97-101. PubMed ID: 1735560
[TBL] [Abstract][Full Text] [Related]
36. [Hereditary renal tumors: Wilms' tumor--congenital anomalies' syndrome].
Tsuchida Y; Yokomori K; Choi SH
Nihon Rinsho; 1995 Nov; 53(11):2742-8. PubMed ID: 8538037
[TBL] [Abstract][Full Text] [Related]
37. Molecular mapping and cloning of the breakpoints of a chromosome 11p14.1-p13 deletion associated with the AGR syndrome.
Gessler M; Bruns GA
Genomics; 1988 Aug; 3(2):117-23. PubMed ID: 2852160
[TBL] [Abstract][Full Text] [Related]
38. 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]
39. Constitutional interstitial deletion of 11p11 and pericentric inversion of chromosome 9 in a patient with Wiedemann-Beckwith syndrome and hepatoblastoma.
Haas OA; Zoubek A; Grümayer ER; Gadner H
Cancer Genet Cytogenet; 1986 Oct; 23(2):95-104. PubMed ID: 3019515
[TBL] [Abstract][Full Text] [Related]
40. Cloning of breakpoints of a chromosome translocation identifies the AN2 locus.
Gessler M; Simola KO; Bruns GA
Science; 1989 Jun; 244(4912):1575-8. PubMed ID: 2544995
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
