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23. Oculocutaneous albinism type 1A: a case report. Karaman A Dermatol Online J; 2008 Nov; 14(11):13. PubMed ID: 19094851 [TBL] [Abstract][Full Text] [Related]
24. Mutations of the P gene in oculocutaneous albinism, ocular albinism, and Prader-Willi syndrome plus albinism. Lee ST; Nicholls RD; Bundey S; Laxova R; Musarella M; Spritz RA N Engl J Med; 1994 Feb; 330(8):529-34. PubMed ID: 8302318 [TBL] [Abstract][Full Text] [Related]
25. Variable expression of vision in sibs with albinism. Summers CG; Creel D; Townsend D; King RA Am J Med Genet; 1991 Sep; 40(3):327-31. PubMed ID: 1951438 [TBL] [Abstract][Full Text] [Related]
26. [Infantile encephalopathies and complex dysmorphies. A case of Rubinstein-Taybi syndrome]. Arnould G; Laxenaire M; Picard L; Andre JM; Brichet B Rev Otoneuroophtalmol; 1970; 42(6):306-12. PubMed ID: 5502128 [No Abstract] [Full Text] [Related]
28. [Three cases of Costello syndrome presenting with intractable epilepsy and profound psychomotor retardation/regression]. Fujikawa Y; Sugai K; Fukumizu M; Hanaoka S; Sasaki M; Kaga M No To Hattatsu; 2001 Sep; 33(5):430-5. PubMed ID: 11558147 [TBL] [Abstract][Full Text] [Related]
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33. [Diagnosis and care of patients with albinism]. Eskina EN; Smol'ianinova IL; Shamshinova AM Vestn Oftalmol; 1994; 110(3):35-8. PubMed ID: 7810043 [No Abstract] [Full Text] [Related]
34. Follow-up of a patient with partial trisomy 9p and partial monosomy 8p; description of physical and psychosocial development. Ausems MG; Van Spijker HG; Dijkhuis HJ; Swanenburg De Veye HF; Bijlsma JB Genet Couns; 1996; 7(1):61-5. PubMed ID: 8652090 [TBL] [Abstract][Full Text] [Related]
35. [Familial syndrome of microcephaly with oculocutaneous albinism and digital anomalies]. Castro-Gago M; Pombo M; Novo I; Tojo R; Peña J An Esp Pediatr; 1983 Aug; 19(2):128-31. PubMed ID: 6660641 [TBL] [Abstract][Full Text] [Related]
36. [Prenatal gene diagnosis of oculocutaneous albinism type I]. Li HY; Wu WI; Zheng H; Duan HL; Chen Z; Chen LM Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2006 Jun; 23(3):280-2. PubMed ID: 16767664 [TBL] [Abstract][Full Text] [Related]
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39. Positive angle kappa: a sign of albinism in patients with congenital nystagmus. Brown SM Am J Ophthalmol; 2004 Oct; 138(4):692-3; author reply 693. PubMed ID: 15488828 [No Abstract] [Full Text] [Related]
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