|
| |
Image Results
Loading...
Loading...
Albinism Oculocutaneous Pages on BioPortfolio:
Results from other life science and pharmaceutical sites:
Oculocutaneous albinism - Genetics Home Reference
Oculocutaneous albinism is a group of conditions that affect coloring ( pigmentation) of the skin, hair, and eyes. Affected individuals typically have very ...
http://ghr.nlm.nih.gov/condition=oculocutaneousalbinism...
|
Albinism - Wikipedia, the free encyclopedia
In oculocutaneous albinism (despite its Latin-derived name meaning "eye-and-skin " albinism), pigment is lacking in the eyes, skin and hair. ...
http://en.wikipedia.org/wiki/Albinism...
|
OMIM - ALBINISM, OCULOCUTANEOUS, TYPE IA; OCA1A
MIM #203100 · Text · Description · Clinical Features · Biochemical Features · Inheritance · Mapping · Molecular Genetics · Diagnosis · Population Genetics ...
http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=203100...
|
Oculocutaneous albinism - Wikipedia, the free encyclopedia
Oculocutaneous albinism is a form of albinism involving the eyes ("oculo-"), skin ("-cutaneous"), and according to some definitions, the hair as well. ...
http://en.wikipedia.org/wiki/Oculocutaneous_albinism...
|
Oculocutaneous Albinism Type 1 -- GeneReviews -- NCBI Bookshelf
Oculocutaneous albinism type 1 (OCA1) is characterized by reduced synthesis of melanin in the skin, hair, and eyes, associated with ocular findings of ...
http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part...
|
AJHG - Rufous Oculocutaneous Albinism in Southern African Blacks ...
The heterogeneous group of disorders known as oculocutaneous albinism (OCA) shares cutaneous and ocular hypopigmentation associated with common ...
http://www.cell.com/AJHG/abstract/S0002-9297(07)60199-2...
|
Oculocutaneous Albinism Type 2 -- GeneReviews -- NCBI Bookshelf
Oculocutaneous albinism type 2 (OCA2) is characterized by hypopigmentation of the skin and hair and the characteristic ocular changes found in all types of ...
http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part...
|
TYR - tyrosinase (oculocutaneous albinism IA) - Genetics Home ...
More than 100 mutations in the TYR gene have been identified in people with oculocutaneous albinism type 1. These mutations disrupt the normal production of ...
http://ghr.nlm.nih.gov/gene=tyr...
|
Oculocutaneous Albinism Type 4 -- GeneReviews -- NCBI Bookshelf
14 Jun 2007 ... Oculocutaneous albinism type 4 (OCA4) is characterized by hypopigmentation of the skin and hair plus the characteristic ocular changes found ...
http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part...
|
hair color - oculocutaneous albinism and griscelli syndrome
The classification of oculocutaneous albinism depends upon the nature of the ... Oculocutaneous albinism type I is an autosomal recessive disorder ...
http://www.keratin.com/as/as004.shtml...
|
|