98 related articles for article (PubMed ID: 5617749)
1. [Albinism in certain clinical and genetic arieties. Study and research on a family].
Morra M
Minerva Oftalmol; 1967; 9(6):202-5. PubMed ID: 5617749
[No Abstract] [Full Text] [Related]
2. Genetic and biochemical evidence for two forms of oculocutaneous albinism in man.
Nance WE; Witkop CJ; Rawls RF
Birth Defects Orig Artic Ser; 1971 Mar; 7(3):125-8. PubMed ID: 5173133
[TBL] [Abstract][Full Text] [Related]
3. [Carrier stigmata of ocular albinism in 3 generations of a Serbian family].
Drincic V; Jeftic R
Bull Mem Soc Fr Ophtalmol; 1977; 89():321-6. PubMed ID: 610819
[No Abstract] [Full Text] [Related]
4. Albinoidism and albinism.
Gragg GW
Birth Defects Orig Artic Ser; 1971 Mar; 7(3):203-4. PubMed ID: 5173147
[No Abstract] [Full Text] [Related]
5. Gingival fibromatosis: study of three generations with consanguinity.
Kharbanda P; Sidhu SS; Panda SK; Deshmukh R
Quintessence Int; 1993 Mar; 24(3):161-4. PubMed ID: 8511274
[TBL] [Abstract][Full Text] [Related]
6. [Study on genetic epidemiology of albinism].
Gong Y; Shao C; Zheng H; Chen B; Guo Y
Yi Chuan Xue Bao; 1994; 21(3):169-72. PubMed ID: 7917429
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Albinism in England.
Jay B; Witkop CJ; King RA
Birth Defects Orig Artic Ser; 1982; 18(6):319-25. PubMed ID: 6816306
[No Abstract] [Full Text] [Related]
9. Homozygosity in piebald trait.
Hultén MA; Honeyman MM; Mayne AJ; Tarlow MJ
J Med Genet; 1987 Sep; 24(9):568-71. PubMed ID: 3669051
[TBL] [Abstract][Full Text] [Related]
10. [Albinism].
Souied E; Cohen SY; Soubrane G; Coscas G
J Fr Ophtalmol; 1994; 17(11):692-705. PubMed ID: 7722231
[No Abstract] [Full Text] [Related]
11. [Human albinism: clinical, genetic, cellular, biochemical and molecular aspects].
Aquaron R
Med Trop (Mars); 2000; 60(4):331-41. PubMed ID: 11436583
[No Abstract] [Full Text] [Related]
12. Amish albinism: a distinctive autosomal recessive phenotype.
Nance WE; Jackson CE; Witkop CJ
Am J Hum Genet; 1970 Sep; 22(5):579-86. PubMed ID: 5516239
[No Abstract] [Full Text] [Related]
13. [Pedigree analysis of two families with Alport's syndrome].
Wässer S; Theile H; Schöne D; Lemme B
Padiatr Grenzgeb; 1980; 19(3):167-71. PubMed ID: 7454376
[No Abstract] [Full Text] [Related]
14. [Ocular albinism].
Valle O
Duodecim; 1982; 98(12):950-7. PubMed ID: 7128487
[No Abstract] [Full Text] [Related]
15. [Hermansky-Pudlak syndrome in a Valais village].
Lattion F; Schneider P; Da Prada M; Lorez HP; Richards JG; Picotti GB; Frenck E
Helv Paediatr Acta; 1983 Dec; 38(5-6):495-512. PubMed ID: 6668200
[TBL] [Abstract][Full Text] [Related]
16. Human albinism.
Jay B; Carruthers J; Treplin MC; Winder AF
Birth Defects Orig Artic Ser; 1976; 12(3):415-26. PubMed ID: 821563
[No Abstract] [Full Text] [Related]
17. [Severely diminished vision in a family with recessive sex-determined heredity].
Welge-Lüssen L; Trojan HJ
Ber Zusammenkunft Dtsch Ophthalmol Ges; 1975; (73):158-62. PubMed ID: 1242903
[No Abstract] [Full Text] [Related]
18. Mutation analysis in a family with oculocutaneous albinism manifesting in the same generation of three branches.
Preising MN; Forster H; Tan H; Lorenz B; de Jong PT; Plomp AS
Mol Vis; 2007 Oct; 13():1851-5. PubMed ID: 17960121
[TBL] [Abstract][Full Text] [Related]
19. [Piebaldism (partial albinism): apropos of 2 cases].
Geerts-Marchandise M; Lachapelle JM
Dermatologica; 1977; 155(3):185-9. PubMed ID: 892124
[No Abstract] [Full Text] [Related]
20. Mutation analysis of the tyrosinase gene in oculocutaneous albinism.
Camand O; Marchant D; Boutboul S; Péquignot M; Odent S; Dollfus H; Sutherland J; Levin A; Menasche M; Marsac C; Dufier JL; Heon E; Abitbol M
Hum Mutat; 2001 Apr; 17(4):352. PubMed ID: 11295837
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
