Inherited chst11/mir3922 deletion is associated with a novel recessive syndrome presenting with skeletal malformation and malignant lymphoproliferative disease
- Sameer S. Chopra
- , Ignaty Leshchiner
- , Hatice Duzkale
- , Heather McLaughlin
- , Monica Giovanni
- , Chengsheng Zhang
- , Nathan Stitziel
- , Joyce Fingeroth
- , Robin M. Joyce
- , Matthew Lebo
- , Heidi Rehm
- , Dana Vuzman
- , Richard Maas
- , Shamil R. Sunyaev
- , Michael Murray
- , Christopher A. Cassa
- Division of Cardiology
- Bursky Center for Human Immunology and Immunotherapy
- Center for Cardiovascular Research
- Roy and Diana Vagelos Division of Biology & Biomedical Sciences (DBBS)
- Institute of Clinical and Translational Sciences (ICTS)
- McDonnell Genome Institute (MGI)
- DBBS - Computational and Systems Biology
- DBBS - Human and Statistical Genetics
- DBBS - Biomedical Informatics and Data Science
- DBBS - Molecular Genetics and Genomics
Research output: Contribution to journal › Article › peer-review
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