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3. 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]
4. 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]
5. X-linked retinal disorders and the Lyon hypothesis. Jay B Trans Ophthalmol Soc U K (1962); 1985; 104 ( Pt 8)():836-44. PubMed ID: 3868876 [TBL] [Abstract][Full Text] [Related]
6. 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]
7. Giant melanin granules in vitiliginous achromia with malignant melanoma. Ortonne JP; Perrot H Acta Derm Venereol; 1978; 58(6):475-80. PubMed ID: 83067 [TBL] [Abstract][Full Text] [Related]
9. X-linked inheritance of ocular albinism with late-onset sensorineural deafness. Winship I; Gericke G; Beighton P Am J Med Genet; 1984 Dec; 19(4):797-803. PubMed ID: 6542750 [TBL] [Abstract][Full Text] [Related]
10. The melanin pigmentary disorder in a family with Hermansky-Pudlak syndrome. Frenk E; Lattion F J Invest Dermatol; 1982 Feb; 78(2):141-3. PubMed ID: 7057049 [TBL] [Abstract][Full Text] [Related]
11. Investigation of a case of oculocutaneous albinism. Jung EG; Anton-Lamprecht I Birth Defects Orig Artic Ser; 1971 Jun; 7(8):26-30. PubMed ID: 5006146 [TBL] [Abstract][Full Text] [Related]
12. Ultrastructural evidence of cell communication between epithelial dark cells and melanocytes in vestibular organs of the human inner ear. Masuda M; Yamazaki K; Kanzaki J; Hosoda Y Anat Rec; 1995 Jun; 242(2):267-77. PubMed ID: 7668412 [TBL] [Abstract][Full Text] [Related]
13. Ultrastructure of giant pigment granules in lentigo simplex. Hirone T; Eryu Y Acta Derm Venereol; 1978; 58(3):223-9. PubMed ID: 78636 [TBL] [Abstract][Full Text] [Related]
17. 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]
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19. Autosomal recessively inherited ocular albinism. A new form of ocular albinism affecting females as severely as males. O'Donnell FE; King RA; Green WR; Witkop CJ Arch Ophthalmol; 1978 Sep; 96(9):1621-5. PubMed ID: 687204 [TBL] [Abstract][Full Text] [Related]
20. X-linked ocular albinism: prevalence and mutations--a national study. Rosenberg T; Schwartz M Eur J Hum Genet; 1998; 6(6):570-7. PubMed ID: 9887374 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]