Evaluating chromosomal mosaicism by array comparative genomic hybridization in hematological malignancies: The proposal of a formula

Cancer Genetics

Volumn 204, Issue 4, 2011, Pages 216-218

  Valli, Roberto ^a   Maserati, Emanuela ^a   Marletta, Cristina ^a   Pressato, Barbara ^a   Lo Curto, Francesco ^a   Pasquali, Francesco ^a  

^a UNIVERSITY OF INSUBRIA   (Italy)

Author keywords

ACGH; Chromosomal mosaicism

Indexed keywords

ANALYTIC METHOD; ARTICLE; BONE MARROW HYPOPLASIA; CASE REPORT; CELL COUNT; CELL NUCLEUS; CHILD; CHROMOSOME ANALYSIS; CHROMOSOME MOSAICISM; CHROMOSOME NUMBER; COMPARATIVE GENOMIC HYBRIDIZATION; CONTROLLED STUDY; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENETIC ALGORITHM; HEMATOLOGIC MALIGNANCY; HUMAN; HUMAN CELL; INTERPHASE; MALE; MATHEMATICAL ANALYSIS; MATHEMATICAL COMPUTING; MICROARRAY ANALYSIS; MOLECULAR PROBE; PRESCHOOL CHILD; PRIORITY JOURNAL; SCHOOL CHILD; SHWACHMAN SYNDROME; THROMBOCYTOPENIA; ALGORITHM; BLOOD DISEASE; GENETICS; METHODOLOGY; MOSAICISM;

ALGORITHMS; COMPARATIVE GENOMIC HYBRIDIZATION; HEMATOLOGIC NEOPLASMS; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MICROARRAY ANALYSIS; MOSAICISM;

EID: 79960051725     PISSN: 22107762     EISSN: 22107770     Source Type: Journal    
DOI: 10.1016/j.cancergen.2011.02.002     Document Type: Article

References (10)

1. Shaffer L.G., Bejjani B.A., Torchia B., et al. The identification of microdeletion syndromes and other chromosome abnormalities: cytogenetic methods of the past, new technologies for the future. Am J Med Genet C Semin Med Genet 2007, 145C:335-345.
2. Edelmann L., Hirschhorn K. Clinical utility of array CGH for the detection of chromosomal imbalances associated with mental retardation and multiple congenital anomalies. Ann N Y Acad Sci 2009, 1151:157-166.
3. Maciejewski J.P., Tiu R.V., O'Keefe C. Application of array-based whole genome scanning technologies as a cytogenetic tool in haematological malignancies. Br J Haematol 2009, 146:479-488.
4. Iourov I.Y., Vorsanova S.G., Iourov Y.B. Chromosomal mosaicism goes global. Mol Cytogenet 2008, 1:26.
5. Menten B., Maas N., Thienpont B., et al. Emerging patterns of cryptic chromosomal imbalance in patients with idiopathic mental retardation and multiple congenital anomalies: a new series of 140 patients and review of published reports. J Med Genet 2006, 43:625-633.
6. Ballif B.C., Rorem E.A., Sundin K., et al. Detection of low-level mosaicism by array CGH in routine diagnostic specimens. Am J Med Genet A 2006, 140A:2757-2767.
7. Cheung S.W., Shaw C.A., Scott D.A., et al. Microarray-based CGH detects chromosomal mosaicism not revealed by conventional cytogenetics. Am J Med Genet A 2007, 143A:1679-1686.
8. Neill N.J., Torchia B.S., Bejjani B.A., et al. Comparative analysis of copy number detection by whole-genome BAC and oligonucleotide array CGH. Mol Cytogenet 2010, 3:11.
9. + cells from patients with low-risk myelodysplastic syndromes reveals cryptic copy number alterations and predicts overall and leukemia-free survival. Blood 2008, 112:3412-3424.
10. Maserati E., Pressato B., Valli R., et al. The route to development of myelodysplastic syndrome/acute myeloid leukaemia in Shwachman-Diamond syndrome: the role of ageing, karyotype instability, and acquired chromosome anomalies. Br J Haematol 2009, 145:190-197.