Feingold syndrome associated with two novel MYCN mutations...

American Journal of Medical Genetics Part A 2008 Vol. 146A; Iss. 17

Feingold syndrome associated with two novel MYCN mutations in sporadic and familial cases including monozygotic twins

Bettina Blaumeiser, Barbara Oehl-Jaschkowitz, Wiktor Borozdin, Jürgen Kohlhase
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Volume:
146A
Year:
2008
Language:
english
Pages:
4
DOI:
10.1002/ajmg.a.32444
File:
PDF, 135 KB
english, 2008
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