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Mutational Analysis of PTPN11 Gene in Taiwanese Children with Noonan Syndrome

✍ Scribed by Chia-Sui Hung; Ju-Li Lin; Yann-Jinn Lee; Shuan-Pei Lin; Mei-Chyn Chao; Fu-Sung Lo


Book ID
117630681
Publisher
Chinese Electronic Periodical Services
Year
2007
Tongue
English
Weight
126 KB
Volume
106
Category
Article
ISSN
0929-6646

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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