File:Oculocutaneous albinism eyes.jpg: Difference between revisions

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(Figure 20: OCA1A patient eyes The image shows the eyes of a patient with OCA1A. The iris is observed to be fully translucent and an ‘almost pink’ colour due to the lack of pigment development. ====Reference==== Grønskov, K., Ek, J. and Brondum-N...)
 
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====Reference====
====Reference====
Grønskov, K., Ek, J. and Brondum-Nielsen, K. (2007). Oculocutaneous albinism. Orphanet Journal of Rare Diseases, 2(1), p.43.
Grønskov, K., Ek, J. and Brondum-Nielsen, K. (2007). Oculocutaneous albinism. Orphanet Journal of Rare Diseases, 2(1), p.43.
[[User:Z8600021|Mark Hill]] ([[User talk:Z8600021|talk]]) 17:12, 30 October 2018 (AEDT) Shown below is the correct referencing format that should have been used here.
{{#pmid:17980020}}


====Copyright====
====Copyright====

Revision as of 17:12, 30 October 2018

Figure 20: OCA1A patient eyes

The image shows the eyes of a patient with OCA1A. The iris is observed to be fully translucent and an ‘almost pink’ colour due to the lack of pigment development.

Reference

Grønskov, K., Ek, J. and Brondum-Nielsen, K. (2007). Oculocutaneous albinism. Orphanet Journal of Rare Diseases, 2(1), p.43.

Mark Hill (talk) 17:12, 30 October 2018 (AEDT) Shown below is the correct referencing format that should have been used here.

Grønskov K, Ek J & Brondum-Nielsen K. (2007). Oculocutaneous albinism. Orphanet J Rare Dis , 2, 43. PMID: 17980020 DOI.

Copyright

© Grønskov et al; licensee BioMed Central Ltd. 2007


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current00:09, 17 October 2018Thumbnail for version as of 00:09, 17 October 2018755 × 113 (15 KB)Z5164785 (talk | contribs)Figure 20: OCA1A patient eyes The image shows the eyes of a patient with OCA1A. The iris is observed to be fully translucent and an ‘almost pink’ colour due to the lack of pigment development. ====Reference==== Grønskov, K., Ek, J. and Brondum-N...

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