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Academic Journal

A Novel Double Homozygous BTD Gene Mutation in a Case of Profound Biotinidase Deficiency.

  • Source: Journal of Pediatric Disease / Türkiye Çocuk Hastalıkları Dergisi. may2023, Vol. 17 Issue 3, p250-252. 3p.

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Idiopathic red lesion: case series

Subjects: Health Care Sciences and Services; gingivitis; idiyopatik

  • Source: Volume: 27, Issue: 3 342-346Anatolian Clinic the Journal of Medical SciencesAnadolu Kliniği Tıp Bilimleri Dergisi

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  • 1-7 of  7 results for ""DEVECİ, Kübra""