Discover open access scientific publications

Search, annotate, share and cite publications

Publications by C. Y. Hung

Mutations inRIT1cause Noonan Syndrome - Additional Functional Evidence and Expanding the Clinical Phenotype

Clinical Genetics

English

A 0.25um High Voltage LDMOSFET for RF Applications and High-Frequency Parameter Extraction

English

Related publications

PTPN11 Mutations in Noonan Syndrome: Molecular Spectrum, Genotype-Phenotype Correlation, and Phenotypic Heterogeneity

American Journal of Human Genetics

English

Marshall-Smith Syndrome: The Expanding Phenotype.

Journal of Medical Genetics

English

Germline-Activating RRAS2 Mutations Cause Noonan Syndrome

American Journal of Human Genetics

English

Expanding the Distinctive Neuroimaging Phenotype of ACTA2 Mutations

American Journal of Neuroradiology

Nuclear Medicine

English

Noonan Syndrome: Clinical Aspects and Molecular Pathogenesis

Molecular Syndromology

English

PNPO Deficiency and Cirrhosis: Expanding the Clinical Phenotype?

Internal Medicine

Molecular Biology

English

Expanding the Clinical Phenotype of the 3q29 Microdeletion Syndrome and Characterization of the Reciprocal Microduplication

Molecular Cytogenetics

Molecular Medicine

Molecular Biology

English

Genotype and Phenotype in Patients With Noonan Syndrome and a RIT1 Mutation

Genetics in Medicine

English

The Clinical Phenotype of Lynch Syndrome Due to Germ-Line PMS2 Mutations

Gastroenterology

Gastroenterology

English