Oculocutaneous albinism associated with multiple malformations and psychomotor retardation
Author:
Publisher
Wiley
Subject
Dermatology,Pediatrics, Perinatology and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1525-1470.2010.01115.x/fullpdf
Reference7 articles.
1. A new oculocerebral syndrome with hypopigmentation;Cross;J Pediatr,1967
2. Oculocerebral syndrome with hypopigmentation;Passarge;Birth Defects,1975
3. An oculocerebral hypopigmentation syndrome;Preus;J Genet Hum,1983
4. An oculocerebral hypopigmentation syndrome: a case report with clinical, histochemical, and ultrastructural findings;Patton;J Med Genet,1987
5. Mutations affecting pigmentation in man: I. Neuroectodermal melanolysosomal discase;Elejalde;Am J Med Genet,1979
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3. Molecular genetic studies and delineation of the oculocutaneous albinism phenotype in the Pakistani population;Orphanet Journal of Rare Diseases;2012-06-26
4. Clinico-epidemiologic features of oculocutaneous albinism in northeast section of Cairo – Egypt;Egyptian Journal of Medical Human Genetics;2010-11
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