PTPN11Mutation Associated with Aortic Dilation and Hypertrophic Cardiomyopathy in a Pediatric Patient with Noonan Syndrome
β Scribed by John L. Jefferies; John W. Belmont; Ricardo Pignatelli; Jeffrey A. Towbin; William J. Craigen
- Publisher
- Springer
- Year
- 2009
- Tongue
- English
- Weight
- 185 KB
- Volume
- 31
- Category
- Article
- ISSN
- 0172-0643
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## Abstract Reports on Noonan syndrome (NS) have documented multiple types of coagulation defects and bleeding diathesis, and a wide range of clinical presentations. Early studies suggested that a large proportion of NS patients have coagulation defects, whereas more recent reports indicate low rat
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