T. Nagornova

Clinical and genetic characteristics and orthopedic manifestations of the Saul–Wilson syndrome in two Russian patients

E. Dadali, V. Kenis, P. Gundorova, 2021 .

Does the c.-14C>T Mutation in the IFITM5 Gene Provide Identical Phenotypes for Osteogenesis Imperfecta Type V? Data from Russia and a Literature Review

R. Khusainova, E. Zakharova, A. Tyurin, 2022, Biomedicines.

Clinical and Genetic Characteristics of COL2A1-Associated Skeletal Dysplasias in 60 Russian Patients: Part I

E. Dadali, E. Zakharova, V. Kenis, 2022, Genes.

Clinical and genetic characteristics of rare variants of acromelic skeletal dysplasias caused by mutations in the FBN1 gene

E. Dadali, V. Kenis, A. Murtazina, 2021, Pediatric Traumatology, Orthopaedics and Reconstructive Surgery.

Сlinical and Radiological Characteristics of Two Patients with Acromesomelic Dysplasia Maroteaux Type with New Mutation in the NRP2 Gene

E. Dadali, O. Shchagina, V. Kenis, 2020 .

Clinical and Genetic Characteristics of Pediatric Patients with Hypophosphatasia in the Russian Population

A. V. Vitebskaya, A. Chernov, O. Glotov, 2022, International journal of molecular sciences.

Clinical, Genetic and Orthopedic Characteristics of Desbuquois Dysplasia

I. Bychkov, E. Dadali, V. Kenis, 2021, Traumatology and Orthopedics of Russia.

Rare IFT140-Associated Phenotype of Cranioectodermal Dysplasia and Features of Diagnostic Journey in Patients with Suspected Ciliopathies

A. Marakhonov, E. Dadali, O. Ryzhkova, 2023, Genes.