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Publications by Gajja S. Salomons

Mutations in TKT Are the Cause of a Syndrome Including Short Stature, Developmental Delay, and Congenital Heart Defects

American Journal of Human Genetics

English

Familial 6p22.2 Duplication Associates With Mild Developmental Delay and Increased SSADH Activity

American Journal of Medical Genetics, Part B, Neuropsychiatric Genetics

Molecular Neuroscience

English

The Baxα:Bcl-2 Ratio Modulates the Response to Dexamethasone in Leukaemic Cells and Is Highly Variable in Childhood Acute Leukaemia

International Journal of Cancer

Cancer Research

English

Unraveling Pathology in Juvenile Alexander Disease: Serial Quantitative MR Imaging and Spectroscopy of White Matter

Nuclear Medicine

Cardiovascular Medicine

English

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