Whole Wiskott-Aldrich syndrome protein gene deletion identified by high throughput sequencing
Author:
Publisher
Spandidos Publications
Subject
Cancer Research,Oncology,Genetics,Molecular Biology,Molecular Medicine,Biochemistry
Cited by 6 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Spectrum of WAS gene mutations in Vietnamese patients with Wiskott–Aldrich syndrome;Pediatrics International;2024-01
2. Exome and genome sequencing for pediatric patients with congenital anomalies or intellectual disability: an evidence-based clinical guideline of the American College of Medical Genetics and Genomics (ACMG);Genetics in Medicine;2021-11
3. A Next-Generation Sequencing Test for Severe Congenital Neutropenia;The Journal of Molecular Diagnostics;2021-02
4. Systematic evidence-based review: outcomes from exome and genome sequencing for pediatric patients with congenital anomalies or intellectual disability;Genetics in Medicine;2020-06
5. When WAS Gene Diagnosis Is Needed: Seeking Clues Through Comparison Between Patients With Wiskott-Aldrich Syndrome and Idiopathic Thrombocytopenic Purpura;Frontiers in Immunology;2019-07-09
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