PubMed (cited) for id: 606952

Year	Number of Results
1966	1
1970	1
1971	1
1978	1
1980	1
1981	1
1986	1
1990	1
1991	2
1997	1
2004	1
2008	1
2024	0

1

Chiang PW, Drautz JM, Tsai AC, Spector E, Clericuzio CL. Chiang PW, et al. Am J Med Genet A. 2008 Nov 15;146A(22):2968-70. doi: 10.1002/ajmg.a.32539. Am J Med Genet A. 2008. PMID: 18925668 No abstract available.

2

Response to Warren's letter.

Hu F, Hanifin JM, Prescott GH, Tongue AC. Hu F, et al. Am J Hum Genet. 1981 May;33(3):479-80. Am J Hum Genet. 1981. PMID: 17948558 Free PMC article. No abstract available.

3

Positive angle kappa: a sign of albinism in patients with congenital nystagmus.

Brodsky MC, Fray KJ. Brodsky MC, et al. Am J Ophthalmol. 2004 Apr;137(4):625-9. doi: 10.1016/j.ajo.2003.11.066. Am J Ophthalmol. 2004. PMID: 15059699

4

Apparent digenic inheritance of Waardenburg syndrome type 2 (WS2) and autosomal recessive ocular albinism (AROA).

Morell R, Spritz RA, Ho L, Pierpont J, Guo W, Friedman TB, Asher JH Jr. Morell R, et al. Hum Mol Genet. 1997 May;6(5):659-64. doi: 10.1093/hmg/6.5.659. Hum Mol Genet. 1997. PMID: 9158138

5

Yellow mutant albinism: cytochemical, ultrastructural, and genetic characterization suggesting multiple allelism.

Hu F, Hanifin JM, Prescott GH, Tongue AC. Hu F, et al. Am J Hum Genet. 1980 May;32(3):387-95. Am J Hum Genet. 1980. PMID: 6770679 Free PMC article.

6

Amish albinism: a distinctive autosomal recessive phenotype.

Nance WE, Jackson CE, Witkop CJ Jr. Nance WE, et al. Am J Hum Genet. 1970 Sep;22(5):579-86. Am J Hum Genet. 1970. PMID: 5516239 Free PMC article. No abstract available.

7

Classification of albinism in man.

Witkop CJ Jr, White JG, Nance WE, Jackson CE, Desnick S. Witkop CJ Jr, et al. Birth Defects Orig Artic Ser. 1971 Jun;7(8):13-25. Birth Defects Orig Artic Ser. 1971. PMID: 5173257

8

Waardenburg's syndrome with fundus and other anomalies.

Goldberg MF. Goldberg MF. Arch Ophthalmol. 1966 Dec;76(6):797-810. doi: 10.1001/archopht.1966.03850010799005. Arch Ophthalmol. 1966. PMID: 4958935 No abstract available.

9

Minimal pigment: a new type of oculocutaneous albinism.

King RA, Wirtschafter JD, Olds DP, Brumbaugh J. King RA, et al. Clin Genet. 1986 Jan;29(1):42-50. doi: 10.1111/j.1399-0004.1986.tb00769.x. Clin Genet. 1986. PMID: 3081286

10

A frequent tyrosinase gene mutation in classic, tyrosinase-negative (type IA) oculocutaneous albinism.

Giebel LB, Strunk KM, King RA, Hanifin JM, Spritz RA. Giebel LB, et al. Proc Natl Acad Sci U S A. 1990 May;87(9):3255-8. doi: 10.1073/pnas.87.9.3255. Proc Natl Acad Sci U S A. 1990. PMID: 1970634 Free PMC article.

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