Makale detayı · 2014
Monoallelic and Biallelic Mutations in MAB21L2 Cause a Spectrum of Major Eye Malformations
Dergi
The American Journal of Human Genetics
OpenAlex
Açık erişim · bronze
Atıf 94
Üst %10
Yüzdelik 96.5%
FWCI 5.78
- Yıl
- 2014
- Tür
- article
Veri kaynağı ayrımı
- YÖKSİS dergi adı The American Journal of Human Genetics
- 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.
94 atıf
OpenAlex cited_by_count (önbellek / veritabanı)
Yerel katalogda bu makaleye atıf yapan 25 yayın (OpenAlex referans eşleşmesi; tam dünya listesi değildir).
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- The Genomics of Arthrogryposis, a Complex Trait: Candidate Genes and Further Evidence for Oligogenic Inheritance 2019
- The Genomics of Arthrogryposis, a Complex Trait: Candidate Genes and Further Evidence for Oligogenic Inheritance 2019
- The Genomics of Arthrogryposis, a Complex Trait:Candidate Genes and Further Evidence for Oligogenic Inheritance 2019
- Paralog Studies Augment Gene Discovery: DDX and DHX Genes 2019
- High Prevalence of Multilocus Pathogenic Variation in Neurodevelopmental Disorders in the Turkish Population 2021
- High prevalence of multilocus pathogenic variation in neurodevelopmental disorders in the Turkish population 2021
- High prevalence of multilocus pathogenic variation in neurodevelopmental disorders in the Turkish population 2021