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1q21.1 What We've Learned: Clinical Findings
1q21.1: What We've Learned about Medical Genetics
1q21.1: Neurological Findings and Brain Imaging Studies
Ongoing Research on 16p11.2 and 1q21.1: from genes and brain cells to behavior
Family Studies and Predictors of Clinical Variability in CNVs
16p11.2: What We've Learned about Medical Genetics
Cardiff Rare Variants Webinar
1q21.1 deletion syndrome - Wikipedia Article Audio
1q21 1 duplication syndrome
The Importance of Microdeletions
Why should chromosome 1 abnormalities be assessed in all patients with MM?
Rare NDD and CNV: The facts and knowledge gaps [Overview of NDD and genetic risks] -Louise Gallagher