130 related articles for article (PubMed ID: 3785879)
1. Nettleship-Falls X-linked ocular albinism with Axenfeld's anomaly. A case report.
Hayakawa M; Kato K; Nakajima A; Yoshiike T; Ogawa H
Ophthalmic Paediatr Genet; 1986 Aug; 7(2):109-14. PubMed ID: 3785879
[TBL] [Abstract][Full Text] [Related]
2. [A Japanese family of Nettleship Falls X-linked ocular albinism].
Hayakawa M; Kanai A; Kato K; Nakajima A; Takamori K
Nippon Ganka Gakkai Zasshi; 1990 Dec; 94(12):1181-7. PubMed ID: 2082739
[TBL] [Abstract][Full Text] [Related]
3. Macromelanosomes in X-linked ocular albinism.
Garner A; Jay BS
Histopathology; 1980 May; 4(3):243-54. PubMed ID: 7390409
[TBL] [Abstract][Full Text] [Related]
4. [Studies of X-linked recessive ocular albinism of the Nettleship-Falls type--with special reference to the association of megalocornea].
Awaya S; Tsunekawa F; Koizumi E; Miyake Y; Yokoyama K
Nippon Ganka Gakkai Zasshi; 1988 Jan; 92(1):146-50. PubMed ID: 3389256
[No Abstract] [Full Text] [Related]
5. X-Linked ocular albinism; Nettleship-Falls ocular albinism.
Booth AV; Soldano AC; Levine J; Pomeranz M
Dermatol Online J; 2008 May; 14(5):4. PubMed ID: 18627740
[TBL] [Abstract][Full Text] [Related]
6. Forsius-Eriksson syndrome: its relation to the Nettleship-Falls X-linked ocular albinism.
O'Donnell FE; Green WR; McKusick VA; Forsius H; Eriksson AW
Clin Genet; 1980 Jun; 17(6):403-8. PubMed ID: 7398111
[TBL] [Abstract][Full Text] [Related]
7. X-linked ocular albinism: relative value of skin biopsy, iris transillumination and funduscopy in identifying affected males and carriers.
Cortin P; Tremblay M; Lemagne JM
Can J Ophthalmol; 1981 Jul; 16(3):121-3. PubMed ID: 7296358
[TBL] [Abstract][Full Text] [Related]
8. X-linked ocular albinism. An oculocutaneous macromelanosomal disorder.
O'Donnell FE; Hambrick GW; Green WR; Iliff WJ; Stone DL
Arch Ophthalmol; 1976 Nov; 94(11):1883-92. PubMed ID: 985163
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. X-linked ocular albinism in Blacks. Ocular albinism cum pigmento.
O'Donnell FE; Green WR; Fleischman JA; Hambrick GW
Arch Ophthalmol; 1978 Jul; 96(7):1189-92. PubMed ID: 666626
[TBL] [Abstract][Full Text] [Related]
11. Aland eye disease: no albino misrouting.
van Dorp DB; Eriksson AW; Delleman JW; van Vliet AG; Collewijn H; van Balen AT; Forsius HR
Clin Genet; 1985 Dec; 28(6):526-31. PubMed ID: 4075563
[TBL] [Abstract][Full Text] [Related]
12. Genetic studies of ocular albinism in a large Virginia kindred.
Szymanski KA; Boughman JA; Nance WE; Olansky DC; Weinberg RS
Ann Ophthalmol; 1984 Feb; 16(2):183-5, 188-91, 194-6 passim. PubMed ID: 6703591
[TBL] [Abstract][Full Text] [Related]
13. Macromelanosomes in X-linked ocular albinism (XLOA).
Yoshiike T; Manabe M; Hayakawa M; Ogawa H
Acta Derm Venereol; 1985; 65(1):66-9. PubMed ID: 2578709
[TBL] [Abstract][Full Text] [Related]
14. X-linked ocular albinism: a family containing a manifesting heterozygote, and an affected male married to a female with autosomal recessive ocular albinism.
Jaeger C; Jay B
Hum Genet; 1981; 56(3):299-304. PubMed ID: 7239514
[TBL] [Abstract][Full Text] [Related]
15. The familial association of neurofibromatosis, peroneal muscular atrophy, congenital deafness, partial albinism, and Axenfeld's defect.
Bradley WG; Richardson J; Frew IJ
Brain; 1974 Sep; 97(3):521-32. PubMed ID: 4213898
[No Abstract] [Full Text] [Related]
16. Axenfeld's anomaly associated with Down's syndrome.
Stokes DW; Parrish CM
Cornea; 1992 Mar; 11(2):163-4. PubMed ID: 1533830
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Genetic counselling in X-linked ocular albinism: clinical features of the carrier state.
Charles SJ; Moore AT; Grant JW; Yates JR
Eye (Lond); 1992; 6 ( Pt 1)():75-9. PubMed ID: 1426406
[TBL] [Abstract][Full Text] [Related]
19. X linked ocular albinism in Japanese patients.
Shiono T; Tsunoda M; Chida Y; Nakazawa M; Tamai M
Br J Ophthalmol; 1995 Feb; 79(2):139-43. PubMed ID: 7696233
[TBL] [Abstract][Full Text] [Related]
20. Oculocutaneous Albinism associated with Axenfeld's Anomaly: Three case reports.
Keshav BR; Mohammed MJ; Mahmood N
Sultan Qaboos Univ Med J; 2010 Apr; 10(1):111-3. PubMed ID: 21509091
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]