ABCC8 (Turkish Wikipedia)

Analysis of information sources in references of the Wikipedia article "ABCC8" in Turkish language version.

Last modified: 11:50:00, 5 February 2026 (UTC)

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adsabs.harvard.edu (Global: 14^th place; Turkish: 32^nd place)

Glaser B, Chiu KC, Anker R, Nestorowicz A, Landau H, Ben-Bassat H, ve diğerleri. (June 1994). "Familial hyperinsulinism maps to chromosome 11p14-15.1, 30 cM centromeric to the insulin gene". Nature Genetics. 7 (2). ss. 185-188. doi:10.1038/ng0694-185. PMID 7920639.
Thomas PM, Cote GJ, Wohllk N, Haddad B, Mathew PM, Rabl W, ve diğerleri. (April 1995). "Mutations in the sulfonylurea receptor gene in familial persistent hyperinsulinemic hypoglycemia of infancy". Science. 268 (5209). ss. 426-429. Bibcode:1995Sci...268..426T. doi:10.1126/science.7716548. PMID 7716548.

"İnsan PubMed Başvurusu:". National Center for Biotechnology Information, U.S. National Library of Medicine.
"Fare PubMed Başvurusu:". National Center for Biotechnology Information, U.S. National Library of Medicine.
Glaser B, Chiu KC, Anker R, Nestorowicz A, Landau H, Ben-Bassat H, ve diğerleri. (June 1994). "Familial hyperinsulinism maps to chromosome 11p14-15.1, 30 cM centromeric to the insulin gene". Nature Genetics. 7 (2). ss. 185-188. doi:10.1038/ng0694-185. PMID 7920639.
Thomas PM, Cote GJ, Wohllk N, Haddad B, Mathew PM, Rabl W, ve diğerleri. (April 1995). "Mutations in the sulfonylurea receptor gene in familial persistent hyperinsulinemic hypoglycemia of infancy". Science. 268 (5209). ss. 426-429. Bibcode:1995Sci...268..426T. doi:10.1126/science.7716548. PMID 7716548.