Benign & Pathological Chromosomal Imbalances systematically clarifies the disease implications of cytogenetically visible copy number variants (CG-CNV) using cytogenetic assessment of heterochromatic or euchromatic DNA variants. While variants of several megabasepair can be present in the human genome without clinical consequence, visually distinguishing these benign areas from disease implications does not always occur to practitioners accustomed to costly molecular profiling methods such as FISH, aCGH, and NGS.
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Benign and Pathological Chromosomal Imbalances : Microscopic and Submicroscopic Copy Number Variations (CNVs) in Genetics and Counseling
RM386.81
Product Details:
Category: Geriatric Medicine
ISBN
9780124046313
Edition
1
Publisher
Elsevier - Health Sciences
Pages
220
Weight
0.52
Please allow 7-15 days for delivery of this item
ISBN | 9780124046313 |
Author | Thomas Liehr |
Publisher | Elsevier - Health Sciences |
Year | 2014 |
Edition | 1 |
Pages | 220 |
Format | Hardback |
Weight | 0.52 kg |
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