The Value of Chromosome Analysis to Interrogate Variants in DNMT3B Causing Immunodeficiency, Centromeric Instability, and Facial Anomaly Syndrome Type I (ICF1).
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Authors
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Kellner, Erinn S1
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Rathbun, Pamela A2
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Marshall, Gary S3
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Tolusso, Leandra K2
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Smolarek, Teresa A2, 4
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Sun, Miao2, 4
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Chandra, Sharat5, 4
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Bleesing, Jack5, 4
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Marsh, Rebecca A5, 4
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1
Division of Bone Marrow Transplantation and Immune Deficiency, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA. [email protected]
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2
Division of Human Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.
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3
Division of Pediatric Infectious Diseases, University of Louisville School of Medicine, Louisville, KY, USA.
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4
Department of Pediatrics, University of Cincinnati, Cincinnati, OH, USA.
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5
Division of Bone Marrow Transplantation and Immune Deficiency, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.
- Type
- Published Article
- Journal
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Journal of Clinical Immunology
- Publisher
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Springer-Verlag
- Publication Date
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Nov 01, 2019
- Volume
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39
- Issue
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8
- Pages
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857–859
- Identifiers
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DOI: 10.1007/s10875-019-00704-6
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PMID: 31686314
- Source
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Medline
- Language
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English
- License
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Unknown
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.
This record was last updated on 09/23/2020 and may not reflect the most current and accurate biomedical/scientific data available from NLM.
The corresponding record at NLM can be accessed at
https://www.ncbi.nlm.nih.gov/pubmed/31686314
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