Albinisme (Norwegian Wikipedia)
Analysis of information sources in references of the Wikipedia article "Albinisme" in Norwegian language version.
refsWebsite
Global rank
Norwegian rank
low place
439th place
low place
low place
low place
low place
49th place
132nd place
5,181st place
low place
6th place
42nd place
albinisme.no
archive.org
- Gunnarsson, Ulrika; Hellström, Anders R.; Tixier-Boichard, Michele; Minvielle, Francis; Bed'hom, Bertrand; Ito, Shin'ichi; Jensen, Per; Rattink, Annemieke; Vereijken, Addie; Andersson, Leif (februar 2007). «Mutations in SLC45A2 Cause Plumage Color Variation in Chicken and Japanese Quail». Genetics. 175 (2): 867–877. PMC 1800597
. PMID 17151254. doi:10.1534/genetics.106.063107.
doi.org
- Gunnarsson, Ulrika; Hellström, Anders R.; Tixier-Boichard, Michele; Minvielle, Francis; Bed'hom, Bertrand; Ito, Shin'ichi; Jensen, Per; Rattink, Annemieke; Vereijken, Addie; Andersson, Leif (februar 2007). «Mutations in SLC45A2 Cause Plumage Color Variation in Chicken and Japanese Quail». Genetics. 175 (2): 867–877. PMC 1800597 . PMID 17151254. doi:10.1534/genetics.106.063107.
- Brilliant, Murray H. (2001). «The Mouse p (pink-eyed dilution) and Human P Genes, Oculocutaneous Albinism Type 2 (OCA2), and Melanosomal pH». Pigment Cell Research. 14 (2): 86–93. PMID 11310796. doi:10.1034/j.1600-0749.2001.140203.x.
nih.gov
ncbi.nlm.nih.gov
- Gunnarsson, Ulrika; Hellström, Anders R.; Tixier-Boichard, Michele; Minvielle, Francis; Bed'hom, Bertrand; Ito, Shin'ichi; Jensen, Per; Rattink, Annemieke; Vereijken, Addie; Andersson, Leif (februar 2007). «Mutations in SLC45A2 Cause Plumage Color Variation in Chicken and Japanese Quail». Genetics. 175 (2): 867–877. PMC 1800597 . PMID 17151254. doi:10.1534/genetics.106.063107.
- Brilliant, Murray H. (2001). «The Mouse p (pink-eyed dilution) and Human P Genes, Oculocutaneous Albinism Type 2 (OCA2), and Melanosomal pH». Pigment Cell Research. 14 (2): 86–93. PMID 11310796. doi:10.1034/j.1600-0749.2001.140203.x.
rarediseases.org
- «Oculocutaneous Albinism». NORD (National Organization for Rare Disorders) (på engelsk). Besøkt 23. juni 2020.