167 related articles for article (PubMed ID: 1968033)
1. A panel of restriction fragment length polymorphisms for chromosomal band 11p13.
Huff V; Compton DA; Strong LC; Saunders GF
Hum Genet; 1990 Feb; 84(3):253-7. PubMed ID: 1968033
[TBL] [Abstract][Full Text] [Related]
2. Long range physical map of the Wilms' tumor-aniridia region on human chromosome 11.
Compton DA; Weil MM; Jones C; Riccardi VM; Strong LC; Saunders GF
Cell; 1988 Dec; 55(5):827-36. PubMed ID: 2847871
[TBL] [Abstract][Full Text] [Related]
3. Parental origin of de novo constitutional deletions of chromosomal band 11p13.
Huff V; Meadows A; Riccardi VM; Strong LC; Saunders GF
Am J Hum Genet; 1990 Jul; 47(1):155-60. PubMed ID: 1971994
[TBL] [Abstract][Full Text] [Related]
4. Autosomal dominant aniridia linked to the chromosome 11p13 markers catalase and D11S151 in a large Dutch family.
Mannens M; Bleeker-Wagemakers EM; Bliek J; Hoovers J; Mandjes I; van Tol S; Frants RR; Heyting C; Westerveld A; Slater RM
Cytogenet Cell Genet; 1989; 52(1-2):32-6. PubMed ID: 2575483
[TBL] [Abstract][Full Text] [Related]
5. Complete physical map of the WAGR region of 11p13 localizes a candidate Wilms' tumor gene.
Rose EA; Glaser T; Jones C; Smith CL; Lewis WH; Call KM; Minden M; Champagne E; Bonetta L; Yeger H
Cell; 1990 Feb; 60(3):495-508. PubMed ID: 2154334
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Molecular nature of genetic changes resulting in loss of heterozygosity of chromosome 11 in Wilms' tumours.
Mannens M; Slater RM; Heyting C; Bliek J; de Kraker J; Coad N; de Pagter-Holthuizen P; Pearson PL
Hum Genet; 1988 Dec; 81(1):41-8. PubMed ID: 2848758
[TBL] [Abstract][Full Text] [Related]
8. A BglII RFLP detected by the probe JA8-1 at human chromosome band 11p13 (D11S417).
Ton CC; Huff V; Weil MM; Strong LC; Saunders GF
Nucleic Acids Res; 1990 Feb; 18(4):1084. PubMed ID: 1969141
[No Abstract] [Full Text] [Related]
9. The importance of DNA analysis in sporadic aniridia.
Mannens M; Hoovers JM; Bleeker-Wagemakers EM; Mäntyjärvi M; Tuppurainen K
Acta Ophthalmol (Copenh); 1993 Dec; 71(6):841-5. PubMed ID: 7908773
[TBL] [Abstract][Full Text] [Related]
10. Alphoid DNA polymorphisms for chromosome 21 can be distinguished from those of chromosome 13 using probes homologous to both.
Jabs EW; Warren AC; Taylor EW; Colyer CR; Meyers DA; Antonarakis SE
Genomics; 1991 Jan; 9(1):141-6. PubMed ID: 1672286
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Definition of the limits of the Wilms tumor locus on human chromosome 11p13.
Compton DA; Weil MM; Bonetta L; Huang A; Jones C; Yeger H; Williams BR; Strong LC; Saunders GF
Genomics; 1990 Feb; 6(2):309-15. PubMed ID: 2155176
[TBL] [Abstract][Full Text] [Related]
13. In situ hybridization mapping and restriction fragment length polymorphism analysis of the porcine albumin (ALB) and transferrin (TF) genes.
Chowdhary BP; Johansson M; Chaudhary R; Ellegren H; Gu F; Andersson L; Gustavsson I
Anim Genet; 1993 Apr; 24(2):85-90. PubMed ID: 8101068
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Nonlinkage of 16q markers to familial predisposition to Wilms' tumor.
Huff V; Reeve AE; Leppert M; Strong LC; Douglass EC; Geiser CF; Li FP; Meadows A; Callen DF; Lenoir G
Cancer Res; 1992 Nov; 52(21):6117-20. PubMed ID: 1356625
[TBL] [Abstract][Full Text] [Related]
16. Correlation of chromosome abnormalities with histological and clinical features in Wilms' and other childhood renal tumors.
Kaneko Y; Homma C; Maseki N; Sakurai M; Hata J
Cancer Res; 1991 Nov; 51(21):5937-42. PubMed ID: 1657374
[TBL] [Abstract][Full Text] [Related]
17. Isolation and characterization of DNA probes from a flow-sorted human chromosome 8 library that detect restriction fragment length polymorphism (RFLP).
Wood S; Starr TV; Shukin RJ
Am J Hum Genet; 1986 Dec; 39(6):744-50. PubMed ID: 2879441
[TBL] [Abstract][Full Text] [Related]
18. Rapid isolation of moderate and highly polymorphic DNA fragments mapping close to WT (Wilms' tumour) and AN2 (aniridia) on chromosome 11.
Boyd PA; Christie S; Hastie ND; Porteous DJ
Hum Genet; 1989 Mar; 81(4):349-52. PubMed ID: 2564837
[TBL] [Abstract][Full Text] [Related]
19. An unreported RFLP for probe 218 EP6 that is useful in linkage analysis of adult polycystic kidney disease.
Jeffery S; Morgan S
Hum Genet; 1993 Oct; 92(4):428. PubMed ID: 7901145
[TBL] [Abstract][Full Text] [Related]
20. The beta-subunit of follicle-stimulating hormone is deleted in patients with aniridia and Wilms' tumour, allowing a further definition of the WAGR locus.
Glaser T; Lewis WH; Bruns GA; Watkins PC; Rogler CE; Shows TB; Powers VE; Willard HF; Goguen JM; Simola KO
Nature; 1986 Jun 26-Jul 2; 321(6073):882-7. PubMed ID: 3014343
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
