PAX3 (Persian Wikipedia)

Analysis of information sources in references of the Wikipedia article "PAX3" in Persian language version.

Last modified: 01:02:38, 2 November 2025 (UTC)

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archive.org (Global: 6^th place; Persian: 4^th place)

Baldwin CT, Hoth CF, Amos JA, da-Silva EO, Milunsky A (February 1992). "An exonic mutation in the HuP2 paired domain gene causes Waardenburg's syndrome". primary. Nature. 355 (6361): 637–8. doi:10.1038/355637a0. PMID 1347149.

Stuart ET, Kioussi C, Gruss P (1994). "Mammalian Pax genes". review. Annual Review of Genetics. 28: 219–36. doi:10.1146/annurev.ge.28.120194.001251. PMID 7893124.
Buckingham M, Relaix F (2007). "The role of Pax genes in the development of tissues and organs: Pax3 and Pax7 regulate muscle progenitor cell functions". review. Annual Review of Cell and Developmental Biology. 23: 645–73. doi:10.1146/annurev.cellbio.23.090506.123438. PMID 17506689.
Baldwin CT, Hoth CF, Amos JA, da-Silva EO, Milunsky A (February 1992). "An exonic mutation in the HuP2 paired domain gene causes Waardenburg's syndrome". primary. Nature. 355 (6361): 637–8. doi:10.1038/355637a0. PMID 1347149.

Stuart ET, Kioussi C, Gruss P (1994). "Mammalian Pax genes". review. Annual Review of Genetics. 28: 219–36. doi:10.1146/annurev.ge.28.120194.001251. PMID 7893124.
Buckingham M, Relaix F (2007). "The role of Pax genes in the development of tissues and organs: Pax3 and Pax7 regulate muscle progenitor cell functions". review. Annual Review of Cell and Developmental Biology. 23: 645–73. doi:10.1146/annurev.cellbio.23.090506.123438. PMID 17506689.
Baldwin CT, Hoth CF, Amos JA, da-Silva EO, Milunsky A (February 1992). "An exonic mutation in the HuP2 paired domain gene causes Waardenburg's syndrome". primary. Nature. 355 (6361): 637–8. doi:10.1038/355637a0. PMID 1347149.

"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.