Aim: The aim of this study was to identify the clinical and immunologic features of patients with 22q11.2 deletion syndrome who were followed up in our clinic Thus, it is aimed to identify the syndrome early, choose the right treatment options according to humoral and cellular immunologic analysis, and enlighten how to follow up these kinds of patients with immunodeficiencies
<p>Clinical and 22q11.2 deletion-related characteristics of individuals with 22q11.2 deletion syndro...
Objective: To investigate humoral compartment at diagnosis and during follow-up in patients with 22q...
Purpose: 22q11.2 deletion syndrome is a contiguous gene deletion syndrome with multisystem involveme...
Objective To investigate the clinical manifestations at diagnosis and during follow-up in patients w...
Objective To investigate the clinical manifestations at diagnosis and during follow-up in patients w...
OBJECTIVE: To investigate the clinical manifestations at diagnosis and during follow-up in patients ...
OBJECTIVE: To investigate the clinical manifestations at diagnosis and during follow-up in patients...
The work represents a family which includes two siblings with chromosome 22q11.2 deletion syndrome. ...
Introduction and objectives: The purpose of this study was to evaluate patients diagnosed with 22q11...
22q11.2 deletion syndrome is the most frequent microdeletion syndrome in humans and caused by hemizy...
<p>Clinical and 22q11.2 deletion-related characteristics of individuals with 22q11.2 deletion syndro...
Objective: To investigate humoral compartment at diagnosis and during follow-up in patients with 22q...
Purpose: 22q11.2 deletion syndrome is a contiguous gene deletion syndrome with multisystem involveme...
Objective To investigate the clinical manifestations at diagnosis and during follow-up in patients w...
Objective To investigate the clinical manifestations at diagnosis and during follow-up in patients w...
OBJECTIVE: To investigate the clinical manifestations at diagnosis and during follow-up in patients ...
OBJECTIVE: To investigate the clinical manifestations at diagnosis and during follow-up in patients...
The work represents a family which includes two siblings with chromosome 22q11.2 deletion syndrome. ...
Introduction and objectives: The purpose of this study was to evaluate patients diagnosed with 22q11...
22q11.2 deletion syndrome is the most frequent microdeletion syndrome in humans and caused by hemizy...
<p>Clinical and 22q11.2 deletion-related characteristics of individuals with 22q11.2 deletion syndro...
Objective: To investigate humoral compartment at diagnosis and during follow-up in patients with 22q...
Purpose: 22q11.2 deletion syndrome is a contiguous gene deletion syndrome with multisystem involveme...