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Retts syndrom (Danish Wikipedia)

Analysis of information sources in references of the Wikipedia article "Retts syndrom" in Danish language version.

refsWebsite
Global rank Danish rank
3nih.gov
4th place
24th place
2doi.org
2nd place
13th place
2wikidata.org
43rd place
3rd place
1rett.dk
low place
low place
1web.archive.org
1st place
1st place
1lundbeckfonden.com
low place
8,915th place

doi.org

  • J D Lewis; Richard Meehan; W J Henzel; I Maurer-Fogy; P Jeppesen; F Klein; Adrian Peter Bird (12. juni 1992), "Purification, sequence, and cellular localization of a novel chromosomal protein that binds to methylated DNA", Cell, 69 (6): 905-14, doi:10.1016/0092-8674(92)90610-O, PMID 1606614, Wikidata Q28265233
  • Ruthie E. Amir; Ignatia B. Van den Veyver; Mimi Wan; Charles Q. Tran; Uta Francke; Huda Zoghbi (1. oktober 1999), "Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2", Nature Genetics, 23 (2): 185-188, doi:10.1038/13810, PMID 10508514, Wikidata Q22337290

lundbeckfonden.com

nih.gov

pubmed.ncbi.nlm.nih.gov

  • J D Lewis; Richard Meehan; W J Henzel; I Maurer-Fogy; P Jeppesen; F Klein; Adrian Peter Bird (12. juni 1992), "Purification, sequence, and cellular localization of a novel chromosomal protein that binds to methylated DNA", Cell, 69 (6): 905-14, doi:10.1016/0092-8674(92)90610-O, PMID 1606614, Wikidata Q28265233
  • Ruthie E. Amir; Ignatia B. Van den Veyver; Mimi Wan; Charles Q. Tran; Uta Francke; Huda Zoghbi (1. oktober 1999), "Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2", Nature Genetics, 23 (2): 185-188, doi:10.1038/13810, PMID 10508514, Wikidata Q22337290

ncbi.nlm.nih.gov

rett.dk

web.archive.org

wikidata.org

  • J D Lewis; Richard Meehan; W J Henzel; I Maurer-Fogy; P Jeppesen; F Klein; Adrian Peter Bird (12. juni 1992), "Purification, sequence, and cellular localization of a novel chromosomal protein that binds to methylated DNA", Cell, 69 (6): 905-14, doi:10.1016/0092-8674(92)90610-O, PMID 1606614, Wikidata Q28265233
  • Ruthie E. Amir; Ignatia B. Van den Veyver; Mimi Wan; Charles Q. Tran; Uta Francke; Huda Zoghbi (1. oktober 1999), "Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2", Nature Genetics, 23 (2): 185-188, doi:10.1038/13810, PMID 10508514, Wikidata Q22337290