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Congenital Heart Disease: Molecular Diagnostics

Congenital Heart Disease: Molecular Diagnostics

Paperback

Series: Methods in Molecular Medicine, Book 126

Medical Reference

ISBN10: 1627038566
ISBN13: 9781627038560
Publisher: Springer Nature
Published: Oct 20 2014
Pages: 278
Weight: 0.91
Height: 0.61 Width: 6.14 Depth: 9.21
Language: English
Prominent researchers and clinicians describe in detail all the latest laboratory techniques currently used to define the molecular genetic basis for congenital malformations of the heart, cardiomyopathies, cardiac tumors, and arrythmias in human patients. In particular, the methods can be used to identify in clinical samples those genetic mutations responsible for such congenital abnormalities as Marfan syndrome, Williams-Beuren Syndrome, Alagille syndrome, Noonan syndrome, and Friedreich ataxia. The authors also discuss the limitations of identifying patients with congenital heart disease using these techniques during both pre- and postnatal periods.

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