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A 3-bp deletion mutation ofPTPN11 in an infant with severe Noonan syndrome including hydrops fetalis and juvenile myelomonocytic leukemia

✍ Scribed by Yoshida, Rie ;Miyata, Masafumi ;Nagai, Toshiro ;Yamazaki, Toshio ;Ogata, Tsutomu


Book ID
101452639
Publisher
John Wiley and Sons
Year
2004
Tongue
English
Weight
185 KB
Volume
128A
Category
Article
ISSN
0148-7299

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