99 related articles for article (PubMed ID: 1303171)
1. Characterization of a YAC containing part or all of the Norrie disease locus.
Chen ZY; Sims KB; Coleman M; Donnai D; Monaco A; Breakefield XO; Davies KE; Craig IW
Hum Mol Genet; 1992 Jun; 1(3):161-4. PubMed ID: 1303171
[TBL] [Abstract][Full Text] [Related]
2. The Norrie disease gene maps to a 150 kb region on chromosome Xp11.3.
Sims KB; Lebo RV; Benson G; Shalish C; Schuback D; Chen ZY; Bruns G; Craig IW; Golbus MS; Breakefield XO
Hum Mol Genet; 1992 May; 1(2):83-9. PubMed ID: 1301161
[TBL] [Abstract][Full Text] [Related]
3. Organization of the human monoamine oxidase genes and long-range physical mapping around them.
Chen ZY; Powell JF; Hsu YP; Breakefield XO; Craig IW
Genomics; 1992 Sep; 14(1):75-82. PubMed ID: 1427833
[TBL] [Abstract][Full Text] [Related]
4. Isolation of a candidate gene for Norrie disease by positional cloning.
Berger W; Meindl A; van de Pol TJ; Cremers FP; Ropers HH; Döerner C; Monaco A; Bergen AA; Lebo R; Warburg M
Nat Genet; 1992 Jun; 1(3):199-203. PubMed ID: 1303235
[TBL] [Abstract][Full Text] [Related]
5. Human monoamine oxidase A and B genes map to Xp 11.23 and are deleted in a patient with Norrie disease.
Lan NC; Heinzmann C; Gal A; Klisak I; Orth U; Lai E; Grimsby J; Sparkes RS; Mohandas T; Shih JC
Genomics; 1989 May; 4(4):552-9. PubMed ID: 2744764
[TBL] [Abstract][Full Text] [Related]
6. A bidirectional YAC walk from the Norrie disease (NDP) locus.
Black GC; Coleman MP; Chen ZY; Nemeth AH; Davies KE; Craig IW
Genomics; 1995 Feb; 25(3):644-9. PubMed ID: 7759098
[TBL] [Abstract][Full Text] [Related]
7. Detection of a new submicroscopic Norrie disease deletion interval with a novel DNA probe isolated by differential Alu PCR fingerprint cloning.
Bergen AA; Wapenaar MC; Schuurman EJ; Diergaarde PJ; Lerach H; Monaco AP; Bakker E; Bleeker-Wagemakers EM; van Ommen GJ
Cytogenet Cell Genet; 1993; 62(4):231-5. PubMed ID: 8440142
[TBL] [Abstract][Full Text] [Related]
8. Physical fine-mapping of a deletion spanning the Norrie gene.
Diergaarde PJ; Wieringa B; Bleeker-Wagemakers EM; Sims KB; Breakefield XO; Ropers HH
Hum Genet; 1989 Dec; 84(1):22-6. PubMed ID: 2606473
[TBL] [Abstract][Full Text] [Related]
9. Sequence analysis and transcript identification within 1.5 MB of DNA deleted together with the NDP and MAO genes in atypical Norrie disease patients presenting with a profound phenotype.
Suárez-Merino B; Bye J; McDowall J; Ross M; Craig IW
Hum Mutat; 2001 Jun; 17(6):523. PubMed ID: 11385715
[TBL] [Abstract][Full Text] [Related]
10. A novel contiguous deletion involving NDP, MAOB and EFHC2 gene in a patient with familial Norrie disease: bilateral blindness and leucocoria without other deficits.
Jia B; Huang L; Chen Y; Liu S; Chen C; Xiong K; Song L; Zhou Y; Yang X; Zhong M
J Genet; 2017 Dec; 96(6):1015-1020. PubMed ID: 29321361
[TBL] [Abstract][Full Text] [Related]
11. Norrie disease and MAO genes: nearest neighbors.
Chen ZY; Denney RM; Breakefield XO
Hum Mol Genet; 1995; 4 Spec No():1729-37. PubMed ID: 8541872
[TBL] [Abstract][Full Text] [Related]
12. Localisation of the gene for Norrie disease to between DXS7 and DXS426 on Xp.
Lindsay S; Thiselton DL; Bateman JB; Ngo JT; Sparkes RS; Coleman M; Davies KE; Bhattacharya SS
Hum Genet; 1992 Jan; 88(3):349-50. PubMed ID: 1733838
[TBL] [Abstract][Full Text] [Related]
13. A yeast artificial chromosome (YAC) contig encompassing the critical region of the X-linked lymphoproliferative disease (XLP) locus.
Lanyi A; Li B; Li S; Talmadge CB; Brichacek B; Davis JR; Kozel BA; Trask B; van den Engh G; Uzvolgyi E; Stanbridge EJ; Nelson DL; Chinault C; Heslop H; Gross TG; Seemayer TA; Klein G; Purtilo DT; Sumegi J
Genomics; 1997 Jan; 39(1):55-65. PubMed ID: 9027486
[TBL] [Abstract][Full Text] [Related]
14. Clinical, biochemical, and neuropsychiatric evaluation of a patient with a contiguous gene syndrome due to a microdeletion Xp11.3 including the Norrie disease locus and monoamine oxidase (MAOA and MAOB) genes.
Collins FA; Murphy DL; Reiss AL; Sims KB; Lewis JG; Freund L; Karoum F; Zhu D; Maumenee IH; Antonarakis SE
Am J Med Genet; 1992 Jan; 42(1):127-34. PubMed ID: 1308352
[TBL] [Abstract][Full Text] [Related]
15. Norrie disease gene is distinct from the monoamine oxidase genes.
Sims KB; Ozelius L; Corey T; Rinehart WB; Liberfarb R; Haines J; Chen WJ; Norio R; Sankila E; de la Chapelle A
Am J Hum Genet; 1989 Sep; 45(3):424-34. PubMed ID: 2773935
[TBL] [Abstract][Full Text] [Related]
16. Characterization and mapping of the mouse NDP (Norrie disease) locus (Ndp).
Battinelli EM; Boyd Y; Craig IW; Breakefield XO; Chen ZY
Mamm Genome; 1996 Feb; 7(2):93-7. PubMed ID: 8835523
[TBL] [Abstract][Full Text] [Related]
17. Norrie disease: linkage analysis using a 4.2-kb RFLP detected by a human ornithine aminotransferase cDNA probe.
Ngo JT; Bateman JB; Cortessis V; Sparkes RS; Mohandas T; Inana G; Spence MA
Genomics; 1989 May; 4(4):539-45. PubMed ID: 2568328
[TBL] [Abstract][Full Text] [Related]
18. Norrie disease resulting from a gene deletion: clinical features and DNA studies.
Donnai D; Mountford RC; Read AP
J Med Genet; 1988 Feb; 25(2):73-8. PubMed ID: 3162283
[TBL] [Abstract][Full Text] [Related]
19. Norrie disease as part of a complex syndrome explained by a submicroscopic deletion of the X chromosome.
Bleeker-Wagemakers EM; Zweije-Hofman I; Gal A
Ophthalmic Paediatr Genet; 1988 Nov; 9(3):137-42. PubMed ID: 3231429
[TBL] [Abstract][Full Text] [Related]
20. A YAC contig in Xp21 containing the adrenal hypoplasia congenita and glycerol kinase deficiency genes.
Walker AP; Chelly J; Love DR; Brush YI; Récan D; Chaussain JL; Oley CA; Connor JM; Yates J; Price DA
Hum Mol Genet; 1992 Nov; 1(8):579-85. PubMed ID: 1301166
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
