PROP1 (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "PROP1" in English language version.

Last modified:

Ref.Un. Ref.Website
Global rank English rank
630th place
326th place
5th place
5th place
2nd place
2nd place
15th place
8th place

doi.org (Global: 2nd place; English: 2nd place)

  • Wu W, Cogan JD, Pfaffle RW, Dasen JS, Frisch H, O'Connell SM, Flynn SE, Brown MR, Mullis PE, Parks JS, Phillips JA III, Rosenfeld MG (Feb 1998). "Mutations in PROP1 cause familial combined pituitary hormone deficiency". Nat Genet. 18 (2): 147–9. doi:10.1038/ng0298-147. PMID 9462743. S2CID 6882625.

ensembl.org (Global: 630th place; English: 326th place)

may2017.archive.ensembl.org

nih.gov (Global: 5th place; English: 5th place)

ncbi.nlm.nih.gov

pubmed.ncbi.nlm.nih.gov

  • Wu W, Cogan JD, Pfaffle RW, Dasen JS, Frisch H, O'Connell SM, Flynn SE, Brown MR, Mullis PE, Parks JS, Phillips JA III, Rosenfeld MG (Feb 1998). "Mutations in PROP1 cause familial combined pituitary hormone deficiency". Nat Genet. 18 (2): 147–9. doi:10.1038/ng0298-147. PMID 9462743. S2CID 6882625.

semanticscholar.org (Global: 15th place; English: 8th place)

api.semanticscholar.org

  • Wu W, Cogan JD, Pfaffle RW, Dasen JS, Frisch H, O'Connell SM, Flynn SE, Brown MR, Mullis PE, Parks JS, Phillips JA III, Rosenfeld MG (Feb 1998). "Mutations in PROP1 cause familial combined pituitary hormone deficiency". Nat Genet. 18 (2): 147–9. doi:10.1038/ng0298-147. PMID 9462743. S2CID 6882625.