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Publications by Christina Lißewski
Activating Mutations of RRAS2 Are a Rare Cause of Noonan Syndrome
American Journal of Human Genetics
Genetics
Related publications
Germline-Activating RRAS2 Mutations Cause Noonan Syndrome
American Journal of Human Genetics
Genetics
Corrigendum: Gain-Of-Function SOS1 Mutations Cause a Distinctive Form of Noonan Syndrome
Nature Genetics
Genetics
Confirmation of EP300 Gene Mutations as a Rare Cause of Rubinstein–Taybi Syndrome
European Journal of Human Genetics
Genetics
NF1 Gene Mutations Are the Major Molecular Event in Neurofibromatosis-Noonan Syndrome
Journal of Neurology & Stroke
NSD1 Mutations Are the Major Cause of Sotos Syndrome and Occur in Some Cases of Weaver Syndrome but Are Rare in Other Overgrowth Phenotypes
American Journal of Human Genetics
Genetics
A Rare Cause of Rhabdomyolysis: Gitelman Syndrome
International Journal of Case Reports and Images
Aortic Aneurysm: A Rare Cause of Ortner’s Syndrome
Journal of Evolution of Medical and Dental Sciences
A Rare Cause of Difficult Intubation: Fraser Syndrome
Istanbul Medical Journal
A Rare Cause of Acute Respiratory Distress Syndrome
Journal of Anesthesia & Critical Care: Open Access