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Three Types of Immunodeficiency, Centromeric Instability, and Facial Anomalies (ICF) Syndrome Identified by Whole-Exome Sequencing in Saudi Hypogammaglobulinemia Patients: Clinical, Molecular, and Cytogenetic Features

JOURNAL OF CLINICAL IMMUNOLOGY (2018)

Journal

JOURNAL OF CLINICAL IMMUNOLOGY

Volume 38, Issue 8, Pages 847-853

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SPRINGER/PLENUM PUBLISHERS

DOI: 10.1007/s10875-018-0569-9

Keywords

ICF; Whole-exome sequencing; Immunodeficiency; Antibody deficiency; Centromeric instability; Facial anomalies; Cytogenetic; DNMT3B; ZBTB24; HELLS

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Three Types of Immunodeficiency, Centromeric Instability, and Facial Anomalies (ICF) Syndrome Identified by Whole-Exome Sequencing in Saudi Hypogammaglobulinemia Patients: Clinical, Molecular, and Cytogenetic Features

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JOURNAL OF CLINICAL IMMUNOLOGY

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Three Types of Immunodeficiency, Centromeric Instability, and Facial Anomalies (ICF) Syndrome Identified by Whole-Exome Sequencing in Saudi Hypogammaglobulinemia Patients: Clinical, Molecular, and Cytogenetic Features

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JOURNAL OF CLINICAL IMMUNOLOGY

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SPRINGER/PLENUM PUBLISHERS

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