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3. Localization of the X-linked ocular albinism gene (OA1) between DXS278/DXS237 and DXS143/DXS16 by linkage analysis. Bergen AA; Samanns C; Van Dorp DB; Ferguson-Smith MA; Gal A; Bleeker-Wagemakers EM Ophthalmic Paediatr Genet; 1990 Sep; 11(3):165-70. PubMed ID: 2280973 [TBL] [Abstract][Full Text] [Related]
4. Multipoint linkage analysis in X-linked ocular albinism of the Nettleship-Falls type. Bergen AA; Samanns C; Schuurman EJ; van Osch L; van Dorp DB; Pinckers AJ; Bakker E; Gal A; van Ommen GJ; Bleeker-Wagemakers EM Hum Genet; 1991 Dec; 88(2):162-6. PubMed ID: 1684563 [TBL] [Abstract][Full Text] [Related]
5. Genetic mapping of the Kallmann syndrome and X linked ocular albinism gene loci. Zhang Y; McMahon R; Charles SJ; Green JS; Moore AT; Barton DE; Yates JR J Med Genet; 1993 Nov; 30(11):923-5. PubMed ID: 8301646 [TBL] [Abstract][Full Text] [Related]
6. Carrier detection in X-linked ocular albinism of the Nettleship-Falls type by DNA analysis. Bergen AA; Schuurman EJ; van den Born LI; Samanns C; van Dorp DB; Pinckers AJ; Bakker E; van Ommen GJ; Gal A; Bleeker-Wagemakers EM Clin Genet; 1992 Mar; 41(3):135-8. PubMed ID: 1348665 [TBL] [Abstract][Full Text] [Related]
7. Genetic mapping of X linked ocular albinism: linkage analysis in British families. Charles SJ; Moore AT; Yates JR J Med Genet; 1992 Aug; 29(8):552-4. PubMed ID: 1355560 [TBL] [Abstract][Full Text] [Related]
8. Refinement of the localization of the X-linked ocular albinism gene. Bergen AA; Zijp P; Schuurman EJ; Bleeker-Wagemakers EM; Apkarian P; van Ommen GJ Genomics; 1993 Apr; 16(1):272-3. PubMed ID: 8486373 [TBL] [Abstract][Full Text] [Related]
9. Genetic mapping of X-linked ocular albinism: linkage analysis in a large Newfoundland kindred. Charles SJ; Green JS; Moore AT; Barton DE; Yates JR Genomics; 1993 Apr; 16(1):259-61. PubMed ID: 8486368 [TBL] [Abstract][Full Text] [Related]
10. Clinical and molecular characterization of a family affected with X-linked ocular albinism (OA1). Lam BL; Fingert JH; Shutt BC; Singleton EM; Merin LM; Brown HH; Sheffield VC; Stone EM Ophthalmic Genet; 1997 Dec; 18(4):175-84. PubMed ID: 9457748 [TBL] [Abstract][Full Text] [Related]
11. OA1 mutations and deletions in X-linked ocular albinism. Schnur RE; Gao M; Wick PA; Keller M; Benke PJ; Edwards MJ; Grix AW; Hockey A; Jung JH; Kidd KK; Kistenmacher M; Levin AV; Lewis RA; Musarella MA; Nowakowski RW; Orlow SJ; Pagon RS; Pillers DA; Punnett HH; Quinn GE; Tezcan K; Wagstaff J; Weleber RG Am J Hum Genet; 1998 Apr; 62(4):800-9. PubMed ID: 9529334 [TBL] [Abstract][Full Text] [Related]
12. Carrier detection in X linked ocular albinism using linked DNA polymorphisms. Charles SJ; Moore AT; Zhang Y; McMahon R; Barton DE; Yates JR Br J Ophthalmol; 1994 Jul; 78(7):539-41. PubMed ID: 7918264 [TBL] [Abstract][Full Text] [Related]
13. X-linked ocular albinism (Nettleship-Falls): a novel 29-bp deletion in exon 1. Carrier detection by ophthalmic examination and DNA analysis. Rudolph G; Meindl A; Bechmann M; Schworm HD; Achatz H; Boergen KP; Kampik A; Berninger T; Meitinger T Graefes Arch Clin Exp Ophthalmol; 2001 Mar; 239(3):167-72. PubMed ID: 11405065 [TBL] [Abstract][Full Text] [Related]
14. An Xp22 microdeletion associated with ocular albinism and ichthyosis: approximation of breakpoints and estimation of deletion size by using cloned DNA probes and flow cytometry. Schnur RE; Trask BJ; van den Engh G; Punnett HH; Kistenmacher M; Tomeo MA; Naids RE; Nussbaum RL Am J Hum Genet; 1989 Nov; 45(5):706-20. PubMed ID: 2573275 [TBL] [Abstract][Full Text] [Related]
15. Intragenic TaqI restriction fragment length polymorphism (RFLP) in CICN4, between the loci for X-linked ocular albinism (OA1) and microphthalmia with linear skin defects syndrome (MLS). Schnur RE; Wick PA Hum Genet; 1995 May; 95(5):594-5. PubMed ID: 7759088 [TBL] [Abstract][Full Text] [Related]
16. Analysis of a terminal Xp22.3 deletion in a patient with six monogenic disorders: implications for the mapping of X linked ocular albinism. Meindl A; Hosenfeld D; Brückl W; Schuffenhauer S; Jenderny J; Bacskulin A; Oppermann HC; Swensson O; Bouloux P; Meitinger T J Med Genet; 1993 Oct; 30(10):838-42. PubMed ID: 8230160 [TBL] [Abstract][Full Text] [Related]
17. Linkage relationship of X-linked juvenile retinoschisis with Xp22.1-p22.3 probes. Sieving PA; Bingham EL; Roth MS; Young MR; Boehnke M; Kuo CY; Ginsburg D Am J Hum Genet; 1990 Oct; 47(4):616-21. PubMed ID: 1977307 [TBL] [Abstract][Full Text] [Related]
18. X-linked ocular albinism and sensorineural deafness: linkage to Xp22.3. Winship IM; Babaya M; Ramesar RS Genomics; 1993 Nov; 18(2):444-5. PubMed ID: 8288253 [TBL] [Abstract][Full Text] [Related]
19. Deletion analysis maps ocular albinism proximal to the steroid sulphatase locus. Bouloux PM; Kirk J; Munroe P; Duke V; Meindl A; Hilson A; Grant D; Carter N; Betts D; Meitinger T Clin Genet; 1993 Apr; 43(4):169-73. PubMed ID: 8330450 [TBL] [Abstract][Full Text] [Related]
20. Analysis of the OA1 gene reveals mutations in only one-third of patients with X-linked ocular albinism. Schiaffino MV; Bassi MT; Galli L; Renieri A; Bruttini M; De Nigris F; Bergen AA; Charles SJ; Yates JR; Meindl A Hum Mol Genet; 1995 Dec; 4(12):2319-25. PubMed ID: 8634705 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]