QuickView for OBSL1;jsessionid=74777E74D95B771606644EC0C3375557 (gene)

1. Natural history of facial and skeletal features from neonatal period to adulthood in a 3M syndrome c…
2. A Rare Cause of Short Stature: 3M Syndrome in a Patient with Novel Mutation in OBSL1 Gene.
3. Binding of Myomesin to Obscurin-Like-1 at the Muscle M-Band Provides a Strategy for Isoform-Specific…
4. Whole-exome analysis of foetal autopsy tissue reveals a frameshift mutation in OBSL1, consistent wit…
5. Whole-exome analysis of foetal autopsy tissue reveals a frameshift mutation in OBSL1, consistent wit…

There were no clinical trials for OBSL1;jsessionid=74777E74D95B771606644EC0C3375557