Inherited CHST11/MIR3922 deletion is associated with a novel recessive syndrome presenting with skeletal malformation and malignant lymphoproliferative disease

Authors

Nathan Stitziel, Washington University School of Medicine in St. Louis
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Journal

Molecular Genetics & Genomic Medicine

Publication Date

2015

Volume

3

Issue

5

Inclusive Pages

413-423

Document Type

Open Access Publication

DOI

10.1002/mgg3.152

Rights and Permissions

Molecular Genetics & Genomic Medicine 2015; 3(5): 413–423 DOI: 10.1002/mgg3.152 Copyright 2015 The Authors. Molecular Genetics & Genomic Medicine published by Wiley Periodicals, Inc.This is an open access article under the term s of the Creative Commons At tribution License, which permits use,distribution and reproduction in any medium, provided the original work is properly cited.

Recommended Citation

Stitziel, Nathan and et al, "Inherited CHST11/MIR3922 deletion is associated with a novel recessive syndrome presenting with skeletal malformation and malignant lymphoproliferative disease." Molecular Genetics & Genomic Medicine. 3, 5. 413-423. (2015).
https://digitalcommons.wustl.edu/open_access_pubs/4271