Identification of non-recurrent submicroscopic genome imbalances: the advantage of genome-wide microarrays over targeted approaches.
Genome-wide analysis of DNA copy-number changes using microarray-based technologies has enabled the detection of de novo cryptic chromosome imbalances in approximately 10% of individuals with mental retardation. So far, the majority of these submicroscopic microdeletions/duplications appear to be un...
主要な著者: | Koolen, D, Sistermans, E, Nilessen, W, Knight, S, Regan, R, Liu, Y, Kooy, R, Rooms, L, Romano, C, Fichera, M, Schinzel, A, Baumer, A, Anderlid, B, Schoumans, J, van Kessel, A, Nordenskjold, M, de Vries, B |
---|---|
フォーマット: | Journal article |
言語: | English |
出版事項: |
2008
|
類似資料
-
A new chromosome 17q21.31 microdeletion syndrome associated with a common inversion polymorphism.
著者:: Koolen, D, 等
出版事項: (2006) -
Whole genome microarrays for the detection of cryptic genomic imbalances in idiopathic learning disability
著者:: Regan, R, 等
出版事項: (2005) -
Submicroscopic chromosomal imbalances contribute to early abortion
著者:: Haibo Li, 等
出版事項: (2018-07-01) -
Idiopathic learning disability and genome imbalance.
著者:: Knight, S, 等
出版事項: (2006) -
Clinical studies on submicroscopic subtelomeric rearrangements: a checklist.
著者:: de Vries, B, 等
出版事項: (2001)