Osteogenesis imperfecta in 140 Turkish families: Molecular spectrum and, comparison of long-term clinical outcome of those with COL1A1/A2 and biallelic variants-Reference-Cited by-同舟云学术

Osteogenesis imperfecta in 140 Turkish families: Molecular spectrum and, comparison of long-term clinical outcome of those with COL1A1/A2 and biallelic variants

Published:2022-02 Issue: Volume:155 Page:116293
ISSN:8756-3282
Container-title:Bone
language:en
Short-container-title:Bone

Author:

Tüysüz Beyhan,Elkanova Leyla,Uludağ Alkaya Dilek,Güleç Çağrı,Toksoy Güven,Güneş Nilay,Yazan Hakan,Bayhan A. Ilhan,Yıldırım Timur,Yeşil Gözde,Uyguner Z. Oya

Funder

Türkiye Bilimsel ve Teknolojik Araştirma Kurumu

Publisher

Elsevier BV

Subject

Histology,Physiology,Endocrinology, Diabetes and Metabolism

Reference57 articles.

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4. Genetic heterogeneity in osteogenesis imperfecta;Sillence;J. Med. Genet.,1979

5. Osteogenesis imperfecta: clinical diagnosis, nomenclature and severity assessment;van Dijk;Am. J. Med. Genet. A,2014

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