Comparative Analyses of Turkish Variome and Widely Used Genomic Variation Databases for the Evaluation of Rare Sequence Variants in Turkish Individuals: Idiopathic Hypogonadotropic Hypogonadism as a Disease Model.

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Kotan L. D.

Journal of clinical research in pediatric endocrinology, cilt.14, ss.293-301, 2022 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 14
  • Basım Tarihi: 2022
  • Doi Numarası: 10.4274/jcrpe.galenos.2022.2022-3-11
  • Dergi Adı: Journal of clinical research in pediatric endocrinology
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, Academic Search Premier, CINAHL, EMBASE, MEDLINE, Directory of Open Access Journals, TR DİZİN (ULAKBİM)
  • Sayfa Sayıları: ss.293-301
  • Anahtar Kelimeler: Allele frequency, Turkish Variome, variant evaluation, genomic variation databases
  • Çukurova Üniversitesi Adresli: Evet