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Publications by Thomas Arbogast

Germline-Activating RRAS2 Mutations Cause Noonan Syndrome

American Journal of Human Genetics
Genetics
2019English

Related publications

Activating Mutations of RRAS2 Are a Rare Cause of Noonan Syndrome

American Journal of Human Genetics
Genetics
2019English

Corrigendum: Gain-Of-Function SOS1 Mutations Cause a Distinctive Form of Noonan Syndrome

Nature Genetics
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2007English

Mosaic Activating Mutations in FGFR1 Cause Encephalocraniocutaneous Lipomatosis

American Journal of Human Genetics
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2016English

LRIG2 Mutations Cause Urofacial Syndrome

American Journal of Human Genetics
Genetics
2013English

Noonan Syndrome

Paediatrica Indonesiana
2018English

Neurofibromatosis-Noonan Syndrome

2020English

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

Clinical Genetics
Genetics
2015English

NF1 Gene Mutations Are the Major Molecular Event in Neurofibromatosis-Noonan Syndrome

Journal of Neurology & Stroke
2017English

NF1 Gene Mutations Represent the Major Molecular Event Underlying Neurofibromatosis-Noonan Syndrome

American Journal of Human Genetics
Genetics
2005English

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