WS Oetting, MH Brilliant, RA King - Molecular Medicine Today, 1996 - Elsevier Oculocutaneous albinism is characterized by a congenital reduction or absence of
melanin pigment in the skin, hair and eyes. The reduction in the hair and skin
results in a change in color but no change in the development of function ... Cited by 23 - Related articles - All 3 versions
- ►fetalneonatal.com S Biswas, IC Lloyd - Archives of disease in childhood, 1999 - fetalneonatal.com Oculocutaneous albinism (OCA) is a heterogenous group of autosomal recessive
disorders affecting melanin synthesis, characterised by congenital
hypopigmentation of the skin, hair, and eyes. Reduced visual acuity, ... Cited by 14 - Related articles - BL Direct - All 9 versions
[CITATION] Ferramentas básicas da genética molecular humana
A Kriss, I Russell-Eggitt, CM Harris, IC Lloyd, … - Ophthalmic Genetics, 1992 - informahealthcare.com ABSTRACT. Genetic, clinical and electrophysiological aspects of albinism are
described. Em- phasis is placed on electrophysiological features which help to
distinguish albinism from other clinical conditions, and on stimulating and ... Cited by 26 - Related articles - All 4 versions
WS Oetting, CG Summers, RA King - Metabolic, pediatric, and systemic ophthalmology (New …, 1994 - ncbi.nlm.nih.gov Several types of hypopigmentation in humans are called albinism. The phenotype
for different types of albinism varies according to the amount of pigment in the
hale, skin and iris, the reduction in visual acuity and the degree of ... Cited by 16 - Related articles - BL Direct - All 2 versions
WS Oetting - Current Opinion in Pediatrics, 1999 - journals.lww.com Albinism William S Oetting, PhD Albinism was one of the first genetic diseases
to be noted in humans, but until relatively recently, little was known of the
molecular mechanisms involved in its pathogenesis. Recent advances have ... Cited by 17 - Related articles - BL Direct - All 2 versions
