Kubra Baskin

A rare case of syndromic severe congenital neutropenia: JAGN1 mutation.

G. Keskindemirci, K. Boztug, Ç. Aydoğmuş, 2020, The Turkish journal of pediatrics.

Extended clinical and immunological phenotype and transplant outcome in CD27 and CD70 deficiency.

Andrew J. Oler, S. Choo, S. Tangye, 2020, Blood.

Does the Hyper IgM Phenotype Affect Prognosis in Ataxia Telangiectasia?

D. Altun, A. Ikinciogullari, C. Aytekin, 2020 .

Perinatal-lethal Gaucher disease can be the underlying cause of congenital ichthyosis

Kubra Baskin, O. Surmeli, M. Bas, 2019 .

Clinical Features and Outcomes of 23 Patients with Wiskott-Aldrich Syndrome: A Single-Center Experience

A. Ikinciogullari, F. Doğu, S. Ceylaner, 2020, Turkish journal of haematology : official journal of Turkish Society of Haematology.