Acute myeloid leukaemia in a case with Tatton-Brown-Rahman syndrome: the peculiarDNMT3AR882 mutation
Author:
Publisher
BMJ
Subject
Genetics (clinical),Genetics
Reference17 articles.
1. The NSD1 and EZH2 overgrowth genes, similarities and differences;Tatton-Brown;Am J Med Genet C Semin Med Genet,2013
2. NUP98/NSD1 characterizes a novel poor prognostic group in acute myeloid leukemia with a distinct HOX gene expression pattern;Hollink;Blood,2011
3. Mutations in the DNA methyltransferase gene DNMT3A cause an overgrowth syndrome with intellectual disability;Tatton-Brown;Nat Genet,2014
4. SETD2 and DNMT3A screen in the Sotos-like syndrome French cohort;Tlemsani;J Med Genet,2016
5. Tatton-Brown-Rahman syndrome due to 2p23 microdeletion;Okamoto;Am J Med Genet A,2016
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1. Expanding the genetic and clinical spectrum of Tatton-Brown-Rahman syndrome in a series of 24 French patients;Journal of Medical Genetics;2024-06-27
2. Clinical Case of Mild Tatton–Brown–Rahman Syndrome Caused by a Nonsense Variant in DNMT3A Gene;Clinics and Practice;2024-05-21
3. The Role of Clonal Hematopoiesis of Indeterminant Potential and DNA (Cytosine-5)-Methyltransferase Dysregulation in Pulmonary Arterial Hypertension and Other Cardiovascular Diseases;Cells;2023-10-26
4. Epigenetic Causes of Overgrowth Syndromes;The Journal of Clinical Endocrinology & Metabolism;2023-07-14
5. Melanoma in a patient with DNMT3A overgrowth syndrome;Molecular Case Studies;2023-04
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