Search

Search Constraints

Start Over You searched for: Subject whole exome sequencing Remove constraint Subject: whole exome sequencing

Search Results

1. Hereditary Haemorrhagic Telangiectasia (HHT) marked by ACVRL1C1120T variant displays Hypopigmented Naevi and frequent bleeding episodes if CYP2C9 co-mutated: clinical notes & rationale of patient registry