Paternal uniparental isodisomy of chromosome 6 causing a complex syndrome including complete IFN-γ receptor 1 deficiency-Reference-Cited by-同舟云学术

Paternal uniparental isodisomy of chromosome 6 causing a complex syndrome including complete IFN-γ receptor 1 deficiency

Published:2010-03 Issue:3 Volume:152A Page:622-629
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Prando Carolina,Boisson-Dupuis Stéphanie,Grant Audrey V.,Kong Xiao-Fei,Bustamante Jacinta,Feinberg Jacqueline,Chapgier Ariane,Rose Yoann,Jannière Lucile,Rizzardi Elena,Zhang Qiuping,Shanahan Catherine M.,Viollet Louis,Lyonnet Stanislas,Abel Laurent,Ruga Ezia Maria,Casanova Jean-Laurent

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.33291/fullpdf

Reference73 articles.

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3. Rhodococcus equi pneumonia in a renal transplant patient: A case report and review of literature;Arya;Clin Transplant,2004

4. Placental mesenchymal dysplasia associated with transient neonatal diabetes mellitus and paternal UPD6;Aviram;Placenta,2008

5. Diagnosis of neonatal and infancy-onset diabetes;Barbetti;Endocr Dev,2007

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