Prenatal Diagnosis of X-Linked Chronic Granulomatous Disease by Percutaneous Umbilical Blood Sampling-Reference-Cited by-同舟云学术

Prenatal Diagnosis of X-Linked Chronic Granulomatous Disease by Percutaneous Umbilical Blood Sampling

Published:2012-10-10 Issue:5 Volume:76 Page:512-518
ISSN:0300-9475
Container-title:Scandinavian Journal of Immunology
language:en
Short-container-title:Scand J Immunol

Author:

Sun J.¹,Wang Y.²,Liu D.¹,Yu Y.¹,Wang J.¹,Ying W.¹,Wang X.¹

Affiliation:

1. Department of Clinical Immunology; Children's Hospital of Fudan University; Shanghai; China

2. Centre of Prenatal Diagnosis; International Peace Maternity and Child Health Hospital; School of Medicine; ShanghaiJiaoTong University; Shanghai; China

Publisher

Wiley

Subject

Immunology,General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-3083.2012.02772.x/fullpdf

Reference19 articles.

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4. A new genetic subgroup of chronic granulomatous disease with autosomal recessive mutations in p40 phox and selective defects in neutrophil NADPH oxidase activity;Matute;Blood,2009

5. Identification of deletion carriers in X-linked chronic granulomatous disease by real-time PCR;Chiriaco;Genet Test Mol Biomarkers,2009

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