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Prenatal detection of Noonan syndrome by mutation analysis of the PTPN11 and the KRAS genes.
Prenatal detection of Noonan syndrome by mutation analysis of the PTPN11 and the KRAS genes.
2010
Arjan C. Houweling
Y.M. de Mooij
I van der Burgt
Helger G. Yntema
Augusta M. A. Lachmeijer
Attie T. J. I. Go
Keywords:
Genetics
Mutation testing
KRAS
Medicine
Prenatal diagnosis
Osteochondrodysplasia
Noonan syndrome
Mutation
PTPN11
Amniocentesis
Correction
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