S. Göktaş Et Al. , "Severe Congenital Neutropenia due to HAX-1 Mutations," In Rare Diseases in Children Focusing on Pediatric Immunology & Neurology , Ankara: Nobel Tıp Kitapevi, 2020, pp.132-146.
Göktaş, S. Et Al. Severe Congenital Neutropenia due to HAX-1 Mutations. 2020. In Rare Diseases in Children Focusing on Pediatric Immunology & Neurology , Nobel Tıp Kitapevi, Ankara, 132-146.
Göktaş, S., Eken, A., & Patıroğlu, T., (2020). Severe Congenital Neutropenia due to HAX-1 Mutations. Rare Diseases in Children Focusing on Pediatric Immunology & Neurology (pp.132-146), Ankara: Nobel Tıp Kitapevi.
Göktaş, SERDAR, AHMET EKEN, And Türkan Patıroğlu. "Severe Congenital Neutropenia due to HAX-1 Mutations." In Rare Diseases in Children Focusing on Pediatric Immunology & Neurology , 132-146. Ankara: Nobel Tıp Kitapevi, 2020
Göktaş, SERDAR Et Al. "Severe Congenital Neutropenia due to HAX-1 Mutations." Rare Diseases in Children Focusing on Pediatric Immunology & Neurology , Nobel Tıp Kitapevi, 2020, pp.132-146.
Göktaş, S. Eken, A. And Patıroğlu, T. (2020) "Severe Congenital Neutropenia due to HAX-1 Mutations", Rare Diseases in Children Focusing on Pediatric Immunology & Neurology . Ankara: Nobel Tıp Kitapevi.
@bookchapter{bookchapter, author ={SERDAR GÖKTAŞ Et Al. }, chaptertitle={Severe Congenital Neutropenia due to HAX-1 Mutations}, booktitle={ Rare Diseases in Children Focusing on Pediatric Immunology & Neurology}, publisher={Nobel Tıp Kitapevi}, city={Ankara},year={2020} }