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INSL4 (Persian Wikipedia)

Analysis of information sources in references of the Wikipedia article "INSL4" in Persian language version.

Last modified:

Ref.Un. Ref.Website
Global rank Persian rank
54nih.gov
5th place
3rd place
31ensembl.org
630th place
387th place
22doi.org
2nd place
2nd place
11semanticscholar.org
15th place
29th place

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

  • Chassin D, Laurent A, Janneau JL, Berger R, Bellet D (Aug 1996). "Cloning of a new member of the insulin gene superfamily (INSL4) expressed in human placenta". Genomics. 29 (2): 465–70. doi:10.1006/geno.1995.9980. PMID 8666396.
  • Veitia R, Laurent A, Quintana-Murci L, Ottolenghi C, Fellous M, Vidaud M, McElreavey K (Oct 1998). "The INSL4 gene maps close to WI-5527 at 9p24.1→p23.3 clustered with two relaxin genes and outside the critical region for the monosomy 9p syndrome". Cytogenet Cell Genet. 81 (3–4): 275–7. doi:10.1159/000015045. PMID 9730618. S2CID 46801238.

ensembl.org (Global: 630th place; Persian: 387th place)

may2017.archive.ensembl.org

nih.gov (Global: 5th place; Persian: 3rd place)

ncbi.nlm.nih.gov

pubmed.ncbi.nlm.nih.gov

  • Chassin D, Laurent A, Janneau JL, Berger R, Bellet D (Aug 1996). "Cloning of a new member of the insulin gene superfamily (INSL4) expressed in human placenta". Genomics. 29 (2): 465–70. doi:10.1006/geno.1995.9980. PMID 8666396.
  • Veitia R, Laurent A, Quintana-Murci L, Ottolenghi C, Fellous M, Vidaud M, McElreavey K (Oct 1998). "The INSL4 gene maps close to WI-5527 at 9p24.1→p23.3 clustered with two relaxin genes and outside the critical region for the monosomy 9p syndrome". Cytogenet Cell Genet. 81 (3–4): 275–7. doi:10.1159/000015045. PMID 9730618. S2CID 46801238.

semanticscholar.org (Global: 15th place; Persian: 29th place)

api.semanticscholar.org

  • Veitia R, Laurent A, Quintana-Murci L, Ottolenghi C, Fellous M, Vidaud M, McElreavey K (Oct 1998). "The INSL4 gene maps close to WI-5527 at 9p24.1→p23.3 clustered with two relaxin genes and outside the critical region for the monosomy 9p syndrome". Cytogenet Cell Genet. 81 (3–4): 275–7. doi:10.1159/000015045. PMID 9730618. S2CID 46801238.