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Publications by Helger G Yntema

Cancer Risk in Patients With Noonan Syndrome Carrying a PTPN11 Mutation

European Journal of Human Genetics

English

Novel and Recurrent CIB2 Variants, Associated With Nonsyndromic Deafness, Do Not Affect Calcium Buffering and Localization in Hair Cells

European Journal of Human Genetics

English

Structural Variation in Xq28: MECP2 Duplications in 1% of Patients With Unexplained XLMR and in 2% of Male Patients With Severe Encephalopathy

European Journal of Human Genetics

English