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.
General
| Imprint: |
HumanaPress
|
| Country of origin: |
United States |
| Series: |
Methods in Molecular Medicine, 126 |
| Release date: |
April 2006 |
| First published: |
2006 |
| Editors: |
Mary Kearns-Jonker
|
| Dimensions: |
235 x 155 x 21mm (L x W x T) |
| Format: |
Hardcover
|
| Pages: |
278 |
| Edition: |
2006 ed. |
| ISBN-13: |
978-1-58829-375-6 |
| Categories: |
Books >
Medicine >
Clinical & internal medicine >
Cardiovascular medicine
|
| LSN: |
1-58829-375-0 |
| Barcode: |
9781588293756 |
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