Albinism Research Today is a free monthly online journal that collates and summarizes the latest research about Albinism, including details on pigmentation, genetic trait, heritability.

Volume 2 (2006), Issue 8 (August)

1. Congenital cataract and macular hypoplasia in humans associated with a de novo mutation in CRYAA and compound heterozygous mutations in P.
   Graefes Arch Clin Exp Ophthalmol, 244(8): 912-9. [Abstract] [Full-text]
2. OCA1 in different ethnic groups of india is primarily due to founder mutations in the tyrosinase gene.
   Ann Hum Genet, 70: 623-30. [Abstract] [Full-text]
3. Crohn's-like colitis, enterocolitis and perianal disease in Hermansky-Pudlak syndrome.
   Colorectal Dis, 8(7): 539-43. [Abstract] [Full-text]
4. Chiasmal misrouting and foveal hypoplasia without albinism.
   Br J Ophthalmol, 90(9): 1098-102. [Abstract] [Full-text]
5. Is autosomal recessive deafness associated with oculocutaneous albinism a "coincidence syndrome"?
   J Hum Genet, 51(8): 716-20. [Abstract] [Full-text]

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