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3. 11p15 ICR1 Partial Deletions Associated with IGF2/H19 DMR Hypomethylation and Silver–Russell Syndrome. Issue 1 (26th October 2016)

5. 15q11.2 Duplication Encompassing Only the UBE3A Gene Is Associated with Developmental Delay and Neuropsychiatric Phenotypes. Issue 7 (July 2015)

9. A bi‐allelic loss‐of‐function SARS1 variant in children with neurodevelopmental delay, deafness, cardiomyopathy, and decompensation during fever. Issue 12 (4th October 2021)

10. A calibrated cell‐based functional assay to aid classification of MLH1 DNA mismatch repair gene variants. Issue 12 (12th September 2022)