Monosomy 10 Mosaicism as an Incidental Finding in Acute Lymphoblastic Leukemia
- PMID: 40152410
- DOI: 10.1002/pbc.31681
Monosomy 10 Mosaicism as an Incidental Finding in Acute Lymphoblastic Leukemia
References
-
- “Principles of Clinical Cytogenetics and Genome Analysis,” In: R. L. Nussbaum, R. R. McInnes, H. F. Willard, eds., Thompson and Thompson Genetics in Medicine. 8th ed (Philadelphia: Elsevier, 2016): 57–74.
-
- R. Hochstenbach, P. J. Krijtenburg, L. T. van der Veken, et al., “Monosomy 20 Mosaicism Revealed by Extensive Karyotyping in Blood and Skin Cells: Case Report and Review of the Literature,” Cytogenetic and Genome Research 144, no. 3 (2014): 155–162.
-
- K. E. Jackson, F. Tsien, and M. Marble, “Phenotypic Features in a Boy With Monosomy 18 Mosaicism,” American Journal of Medical Genetics 95, no. 3 (2000): 229–232.
-
- Y. B. Yurov, S. G. Vorsanova, I. Y. Iourov, et al., “Unexplained Autism Is Frequently Associated with Low‐level Mosaic Aneuploidy,” Journal of Medical Genetics 44, no. 8 (2007): 521–525.
-
- National Organization for Rare Disorders. Chromosome 10, Monosomy 10p. rarediseases.org.
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