Makale detayı · 2021 · article
Long-Term Follow-Up Outcomes of 19 Patients with Osteogenesis Imperfecta Type XI and Bruck Syndrome Type I Caused by FKBP10 Variants
ISSN0171-967X
YÖKSİS
OpenAlex
Yıl2021
Atıf11OpenAlex
Atıf11Semantic Scholar
Yüzdelik%80,6
FWCI1,221,00 = dünya ortalaması
Scopus (SJR)Q1
WoS (JCR)Q3
Veri kaynağı ayrımı
- YÖKSİSYÖKSİS makale kaydı
- YÖKSİS dergi adıCalcified Tissue International
- Katalog eşleşmesi (ISSN)Calcified Tissue International
- OpenAlexOpenAlex zenginleştirmesi (özet, atıf, konular)
- Semantic Scholaratıf sayısı (OpenAlex ile birleştirilmez)
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11atıfOpenAlex · cited_by_count (önbellek / veritabanı)
Yerel katalogda bu makaleye atıf yapan 11 yayın (OpenAlex referans eşleşmesi; tam dünya listesi değildir).
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- 2022 Osteogenesis imperfecta in 140 Turkish families: Molecular spectrum and, comparison of long-term clinical outcome of those with COL1A1/A2 and biallelic variantsAtıf 28 · OpenAlex
- 2022 Osteogenesis imperfecta in 140 Turkish families: Molecular spectrum and, comparison of long-term clinical outcome of those with COL1A1/A2 and biallelic variantsAtıf 28 · OpenAlex
- 2022 Osteogenesis imperfecta in 140 Turkish families: Molecular spectrum and, comparison of long-term clinical outcome of those with COL1A1/A2 and biallelic variantsAtıf 28 · OpenAlex
- 2025 Investigation of oral health findings and genotype correlations in osteogenesis imperfecta.Atıf 0 · OpenAlex
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- 2024 Investigation of oral health findings and genotype correlations in osteogenesis imperfectaAtıf 0 · OpenAlex