FAM46A (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "FAM46A" in English language version.

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4th place
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1,626th place
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doi.org

  • Barragán I, Borrego S, Abd El-Aziz MM, El-Ashry MF, Abu-Safieh L, Bhattacharya SS, Antiñolo G (January 2008). "Genetic analysis of FAM46A in Spanish families with autosomal recessive retinitis pigmentosa: characterisation of novel VNTRs". Annals of Human Genetics. 72 (Pt 1): 26–34. doi:10.1111/j.1469-1809.2007.00393.x. PMID 17803723. S2CID 2087472.
  • Cui J, Wang W, Wang M, Lin J, Ma Y, Ruan WJ, Xu J, Lai MD (July 2006). "[VNTR polymorphism of C6orf37 in Chinese population]". Zhejiang da Xue Xue Bao. Yi Xue Ban = Journal of Zhejiang University. Medical Sciences. 35 (4): 354–9. doi:10.3785/j.issn.1008-9292.2006.04.002. PMID 16924696.

ensembl.org

May2017.archive.ensembl.org

genecards.org

nih.gov

ncbi.nlm.nih.gov

  • "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  • "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  • "NCBI Gene". NCBI. National Center for Biotechnology Information.
  • "FAM46A Ace View". AceView. NCBI. Retrieved 3 March 2015.
  • "FAM46A Ace View". AceView. NCBI. Retrieved 3 March 2015.

pubmed.ncbi.nlm.nih.gov

  • Barragán I, Borrego S, Abd El-Aziz MM, El-Ashry MF, Abu-Safieh L, Bhattacharya SS, Antiñolo G (January 2008). "Genetic analysis of FAM46A in Spanish families with autosomal recessive retinitis pigmentosa: characterisation of novel VNTRs". Annals of Human Genetics. 72 (Pt 1): 26–34. doi:10.1111/j.1469-1809.2007.00393.x. PMID 17803723. S2CID 2087472.
  • Cui J, Wang W, Wang M, Lin J, Ma Y, Ruan WJ, Xu J, Lai MD (July 2006). "[VNTR polymorphism of C6orf37 in Chinese population]". Zhejiang da Xue Xue Bao. Yi Xue Ban = Journal of Zhejiang University. Medical Sciences. 35 (4): 354–9. doi:10.3785/j.issn.1008-9292.2006.04.002. PMID 16924696.

proteinatlas.org

semanticscholar.org

api.semanticscholar.org

  • Barragán I, Borrego S, Abd El-Aziz MM, El-Ashry MF, Abu-Safieh L, Bhattacharya SS, Antiñolo G (January 2008). "Genetic analysis of FAM46A in Spanish families with autosomal recessive retinitis pigmentosa: characterisation of novel VNTRs". Annals of Human Genetics. 72 (Pt 1): 26–34. doi:10.1111/j.1469-1809.2007.00393.x. PMID 17803723. S2CID 2087472.