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Mutational analysis of the PTPN11 gene in Egyptian patients with Noonan syndrome

✍ Scribed by Essawi, Mona L.; Ismail, Manal F.; Afifi, Hanan H.; Kobesiy, Maha M.; El Kotoury, Ahmed; Barakat, Maged M.


Book ID
122631196
Publisher
Chinese Electronic Periodical Services
Year
2013
Tongue
English
Weight
704 KB
Volume
112
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