Found: 4
Select item for more details and to access through your institution.
Identification of von Willebrand disease type 1 in a patient with Ehlers-Danlos syndrome classic type.
- Published in:
- Haemophilia, 2016, v. 22, n. 4, p. e309, doi. 10.1111/hae.12931
- By:
- Publication type:
- Article
The Abcc6a Knockout Zebrafish Model as a Novel Tool for Drug Screening for Pseudoxanthoma Elasticum.
- Published in:
- Frontiers in Pharmacology, 2022, v. 13, p. 1, doi. 10.3389/fphar.2022.822143
- By:
- Publication type:
- Article
Next Generation Sequencing to Determine the Cystic Fibrosis Mutation Spectrum in Palestinian Population.
- Published in:
- Disease Markers, 2015, v. 2015, p. 1, doi. 10.1155/2015/458653
- By:
- Publication type:
- Article
Mutations in Fibrillin-1 Cause Congenital Scleroderma: Stiff Skin Syndrome.
- Published in:
- Science Translational Medicine, 2010, v. 2, n. 23, p. 1, doi. 10.1126/scitranslmed.3000488
- By:
- Publication type:
- Article