112 related articles for article (PubMed ID: 15991334)
1. Gene symbol: TYR. Disease: Albinism, oculocutaneous 1.
Ray K; Chaki M; Mukhopadhyay A
Hum Genet; 2005 May; 116(6):545. PubMed ID: 15991334
[No Abstract] [Full Text] [Related]
2. Gene symbol: TYR. Disease: Albinism, oculocutaneous 1.
Ray K; Chaki M; Mukhopadhyay A
Hum Genet; 2005 May; 116(6):544. PubMed ID: 15991332
[No Abstract] [Full Text] [Related]
3. Novel human pathological mutations. Gene symbol: TYR. Disease: albinism, oculocutaneous 1.
Ray K; Chaki M; Sengupta M
Hum Genet; 2007 Dec; 122(5):555. PubMed ID: 18383608
[No Abstract] [Full Text] [Related]
4. Gene symbol: TYR. Disease: Albinism, oculocutaneous 1.
Patrosso MC; Lando G; Penco S
Hum Genet; 2008 Oct; 124(3):294. PubMed ID: 18846608
[No Abstract] [Full Text] [Related]
5. Gene symbol: TYR. Disease: Albinism, oculocutaneous 1.
Ray K; Chaki M; Mukhopadhyay A
Hum Genet; 2005 Jul; 117(2-3):299. PubMed ID: 16156027
[No Abstract] [Full Text] [Related]
6. Gene symbol: TYR. Disease: Albinism, oculocutaneous 1.
Ray K; Chaki M; Mukhopadhyay A
Hum Genet; 2005 May; 116(6):544. PubMed ID: 15991333
[No Abstract] [Full Text] [Related]
7. Gene symbol: TYR. Disease: Albinism, oculocutaneous 1.
Ray K; Chaki M; Mukhopadhyay A
Hum Genet; 2005 May; 116(6):533. PubMed ID: 15838715
[No Abstract] [Full Text] [Related]
8. Novel human pathological mutations. Gene symbol: TYR. Disease: albinism, oculocutaneous 1.
Saxena R; Verma IC
Hum Genet; 2010 Apr; 127(4):488. PubMed ID: 21491618
[No Abstract] [Full Text] [Related]
9. Temperature sensitive oculocutaneous albinism associated with missense changes in the tyrosinase gene.
Wang T; Waters CT; Jakins T; Yates JR; Trump D; Bradshaw K; Moore AT
Br J Ophthalmol; 2005 Oct; 89(10):1383-4. PubMed ID: 16170149
[No Abstract] [Full Text] [Related]
10. Novel human pathological mutations. Gene symbol: TYR. Disease: tyrosinase deficiency.
Ray K; Chaki M; Sengupta M
Hum Genet; 2007 Dec; 122(5):556. PubMed ID: 18383611
[No Abstract] [Full Text] [Related]
11. Novel human pathological mutations. Gene symbol: TYR. Disease: tyrosinase deficiency.
Ray K; Chaki M; Sengupta M
Hum Genet; 2007 Dec; 122(5):556. PubMed ID: 18383610
[No Abstract] [Full Text] [Related]
12. Novel human pathological mutations. Gene symbol: TYR. Disease: tyrosinase deficiency.
Ray K; Chaki M; Sengupta M
Hum Genet; 2007 Dec; 122(5):555. PubMed ID: 18383609
[No Abstract] [Full Text] [Related]
13. Novel mutations of the tyrosinase (TYR) gene in type I oculocutaneous albinism (OCA1).
Spritz RA; Oh J; Fukai K; Holmes SA; Ho L; Chitayat D; France TD; Musarella MA; Orlow SJ; Schnur RE; Weleber RG; Levin AV
Hum Mutat; 1997; 10(2):171-4. PubMed ID: 9259202
[No Abstract] [Full Text] [Related]
14. Mutations of the human tyrosinase gene associated with tyrosinase related oculocutaneous albinism (OCA1). Mutations in brief no. 204. Online.
Oetting WS; Fryer JP; King RA
Hum Mutat; 1998; 12(6):433-4. PubMed ID: 10671066
[TBL] [Abstract][Full Text] [Related]
15. Detection of 53 novel DNA variations within the tyrosinase gene and accumulation of mutations in 17 patients with albinism.
Opitz S; Käsmann-Kellner B; Kaufmann M; Schwinger E; Zühlke C
Hum Mutat; 2004 Jun; 23(6):630-1. PubMed ID: 15146472
[TBL] [Abstract][Full Text] [Related]
16. Novel human pathological mutations. Gene symbol: OCA2. Disease: albinism, oculocutaneous II.
Renugadevi K; Sil AK; Perumalsamy V; Sundaresan P
Hum Genet; 2009 Apr; 125(3):340. PubMed ID: 19309806
[No Abstract] [Full Text] [Related]
17. Gene symbol: TYR. Disease: albinism, oculocutaneous 1.
Ray K; Chaki M; Sengupta M
Hum Genet; 2006 Jul; 119(6):675. PubMed ID: 17128464
[No Abstract] [Full Text] [Related]
18. [Oculocutaneous albinism 1B associated with a new mutation in the TYR gene].
Vidal-Ríos P; Fernández-Seara MJ; Cortés E; Hurtado L; Couce ML
An Pediatr (Barc); 2013 May; 78(5):339-40. PubMed ID: 23085315
[No Abstract] [Full Text] [Related]
19. [New nonsense mutation (p.E250X) in the tyrosinase gene of a patient with oculocutaneous albinism type 1A].
Aquaron R; Hesse S; Badens C; Bonerandi JJ
Ann Dermatol Venereol; 2009 Jan; 136(1):57-9. PubMed ID: 19171234
[No Abstract] [Full Text] [Related]
20. [Mutation screening of the TYR and P gene in three patients with oculocutaneous albinism].
Dai C; Li W; Gao B; Li LY; Lu GX
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Aug; 25(4):373-7. PubMed ID: 18683130
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]