Format
Items per page
Sort by

Send to:

Choose Destination

Results: 1 to 20 of 101

Similar articles for PubMed (Select 687204)

1.

Autosomal recessively inherited ocular albinism. A new form of ocular albinism affecting females as severely as males.

O'Donnell FE Jr, King RA, Green WR, Witkop CJ Jr.

Arch Ophthalmol. 1978 Sep;96(9):1621-5.

PMID:
687204
2.

Albinism, or the NOACH syndrome (the book of Enoch c.v. 1-20).

van Dorp DB.

Clin Genet. 1987 Apr;31(4):228-42.

PMID:
3109790
3.

X-linked ocular albinism. An oculocutaneous macromelanosomal disorder.

O'Donnell FE Jr, Hambrick GW Jr, Green WR, Iliff WJ, Stone DL.

Arch Ophthalmol. 1976 Nov;94(11):1883-92.

PMID:
985163
4.

X-linked ocular albinism in Blacks. Ocular albinism cum pigmento.

O'Donnell FE Jr, Green WR, Fleischman JA, Hambrick GW.

Arch Ophthalmol. 1978 Jul;96(7):1189-92.

PMID:
666626
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.

PMID:
6703591
7.

A comprehensive genetic study of autosomal recessive ocular albinism in Caucasian patients.

Hutton SM, Spritz RA.

Invest Ophthalmol Vis Sci. 2008 Mar;49(3):868-72. doi: 10.1167/iovs.07-0791.

PMID:
18326704
8.

[Ocular albinism].

Valle O.

Duodecim. 1982;98(12):950-7. Finnish. No abstract available.

PMID:
7128487
9.

Brown oculocutaneous albinism. Clinical, ophthalmological, and biochemical characterization.

King RA, Lewis RA, Townsend D, Zelickson A, Olds DP, Brumbaugh J.

Ophthalmology. 1985 Nov;92(11):1496-505.

PMID:
3935994
10.

Ophthalmic features of minimal pigment oculocutaneous albinism.

Summers CG, King RA.

Ophthalmology. 1994 May;101(5):906-14.

PMID:
8190479
11.
12.

Macromelanosomes in X-linked ocular albinism.

Garner A, Jay BS.

Histopathology. 1980 May;4(3):243-54.

PMID:
7390409
13.

Macromelanosomes in X-linked ocular albinism (XLOA).

Yoshiike T, Manabe M, Hayakawa M, Ogawa H.

Acta Derm Venereol. 1985;65(1):66-9.

PMID:
2578709
14.

X-linked ocular albinism.

Walker BA, Martyn LJ, Coffman T.

Birth Defects Orig Artic Ser. 1971 Mar;7(3):200-2. No abstract available.

PMID:
5173146
15.

[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. French. No abstract available.

PMID:
610819
16.

X linked ocular albinism in Japanese patients.

Shiono T, Tsunoda M, Chida Y, Nakazawa M, Tamai M.

Br J Ophthalmol. 1995 Feb;79(2):139-43.

17.
18.

Molecular basis of albinism in India: evaluation of seven potential candidate genes and some new findings.

Mondal M, Sengupta M, Samanta S, Sil A, Ray K.

Gene. 2012 Dec 15;511(2):470-4. doi: 10.1016/j.gene.2012.09.012. Epub 2012 Sep 23.

PMID:
23010199
19.

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 24;330(8):529-34.

20.

Minimal pigment: a new type of oculocutaneous albinism.

King RA, Wirtschafter JD, Olds DP, Brumbaugh J.

Clin Genet. 1986 Jan;29(1):42-50.

PMID:
3081286
Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk