Benign and Pathological Chromosomal Imbalances : Microscopic and Submicroscopic Copy Number Variations (CNVs) in Genetics and Counseling

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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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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

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.

ISBN9780124046313
AuthorThomas Liehr
PublisherElsevier - Health Sciences
Year2014
Edition1
Pages220
FormatHardback
Weight0.52 kg

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Benign and Pathological Chromosomal Imbalances : Microscopic and Submicroscopic Copy Number Variations (CNVs) in Genetics and Counseling Benign and Pathological Chromosomal Imbalances : Microscopic and Submicroscopic Copy Number Variations (CNVs) in Genetics and Counseling
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Benign and Pathological Chromosomal Imbalances : Microscopic and Submicroscopic Copy Number Variations (CNVs) in Genetics and Counseling

Please allow 7-15 days for delivery of this item

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