A 3-bp deletion mutation of PTPN11 in an infant with severe...

A 3-bp deletion mutation of PTPN11 in an infant with severe Noonan syndrome including hydrops fetalis and juvenile myelomonocytic leukemia

Rie Yoshida, Masafumi Miyata, Toshiro Nagai, Toshio Yamazaki, Tsutomu Ogata
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Volume:
128A
Year:
2004
Language:
english
Pages:
4
DOI:
10.1002/ajmg.a.30029
File:
PDF, 185 KB
english, 2004
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