Molecular diagnosis of chronic granulomatous disease

Functional and genetic characterization of two extremely rare cases of Williams–Beuren Syndrome associated with chronic granulomatous disease

(2013) Marie J Stasia et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Clinical, functional, and genetic characterization of chronic granulomatous disease in 89 Turkish patients

(2013) Mustafa Yavuz Köker et al.   JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY

Rare Duplication or Deletion of Exons 6, 7 and 8 in CYBB Leading to X-Linked Chronic Granulomatous Disease in Two Patients from Different Families

(2012) Marie José Stasia et al.   JOURNAL OF CLINICAL IMMUNOLOGY

Rapid Genetic Analysis of X-Linked Chronic Granulomatous Disease by High-Resolution Melting

(2010) Harry R. Hill et al.   JOURNAL OF MOLECULAR DIAGNOSTICS

Residual NADPH Oxidase and Survival in Chronic Granulomatous Disease

(2010) Douglas B. Kuhns et al.   NEW ENGLAND JOURNAL OF MEDICINE

A new genetic subgroup of chronic granulomatous disease with autosomal recessive mutations in p40phox and selective defects in neutrophil NADPH oxidase activity

(2009) J. D. Matute et al.   BLOOD

Four differentNCF2mutations in six families from Turkey and an overview ofNCF2gene mutations

(2009) M. Y. Köker et al.   EUROPEAN JOURNAL OF CLINICAL INVESTIGATION

Molecular characterization of a large cohort of patients with Chronic Granulomatous Disease and identification of novel CYBB mutations: An Italian multicenter study

(2009) Gigliola Di Matteo et al.   MOLECULAR IMMUNOLOGY

The array CGH and its clinical applications

(2008) Marwan Shinawi et al.   DRUG DISCOVERY TODAY

Remarks on the article Genetics and immunopathology of chronic granulomatous disease by Marie José Stasia and Xing Jun Li

(2008) Joachim Roesler   Seminars in Immunopathology