Makale detayı · 2010
Identification of a novel dentin matrix protein 1 DMP 1 mutation and dental anomalies in a kindred with autosomal recessive hypophosphatemia
YÖKSİS
OpenAlex
Açık erişim · bronze
SJR Q1
JCR Q1
Atıf 64
Yüzdelik 82.6%
FWCI 1.6
- Yıl
- 2010
- Tür
- article
Veri kaynağı ayrımı
- YÖKSİS YÖKSİS makale kaydı
- YÖKSİS dergi adı Bone
- Katalog eşleşmesi (ISSN) Bone
- OpenAlex OpenAlex zenginleştirmesi (özet, atıf, konular)
Özet
Özet henüz derlenmedi; DergiPark / OpenAlex kuyruğu işlenince burada görünecek.
Konular
Atıflar
OpenAlex cited_by_count. WoS veya Scopus atıf sayısı değildir; o kaynaklar için ayrı kolon yoktur.
64 atıf
OpenAlex cited_by_count (önbellek / veritabanı)
Yerel katalogda bu makaleye atıf yapan 21 yayın (OpenAlex referans eşleşmesi; tam dünya listesi değildir).
- Nationwide Turkish Cohort Study of Hypophosphatemic Rickets 2020
- Management of Systemic Hypersensitivity Reactions to Gonadotropin-Releasing Hormone Analogues during Treatment of Central Precocious Puberty 2020
- A Rare Cause of Hypophosphatemia: Raine Syndrome Changing Clinical Features with Age 2020
- Nationwide Turkish Cohort Study of Hypophosphatemic Rickets 2020
- Nationwide Turkish Cohort Study of Hypophosphatemic Rickets 2020
- A rare cause of hypertension in childhood: Questions 2020
- Management of Systemic Hypersensitivity Reactions to Gonadotropin-Releasing Hormone Analogues during Treatment of Central Precocious Puberty 2020
- Nationwide Turkish Cohort Study of Hypophosphatemic Rickets 2020
- Nationwide Turkish Cohort Study of Hypophosphatemic Rickets 2020
- Magnetic resonance spectroscopy to assess hepatic steatosis in patients with lipodystrophy 2020