13 results on '"Pariani, Mitchel"'
Search Results
2. Images in Vascular Medicine: Vascular complications in a young patient with vascular Ehlers–Danlos syndrome
3. Abstract 17417: Pathogenic and Likely Pathogenic Missense Variants in Cardiovascular Disease Genes Cluster Around Functional Domains
4. Finding missed cases of familial hypercholesterolemia in health systems using machine learning
5. Clinically impactful differences in variant interpretation between clinicians and testing laboratories: a single-center experience
6. Visceroptosis of the bowel in the hypermobility type of Ehlers–Danlos syndrome: Presentation of a rare manifestation and review of the literature
7. A 785 kb deletion of 3p14.1p13, including the FOXP1 gene, associated with speech delay, contractures, hypertonia and blepharophimosis
8. Vascular and connective tissue anomalies associated with X-linked periventricular heterotopia due to mutations in Filamin A
9. Connective tissue spectrum abnormalities associated with spontaneous cerebrospinal fluid leaks: a prospective study
10. Genetic screening in the Persian Jewish community: A pilot study
11. A 785kb deletion of 3p14.1p13, including the FOXP1 gene, associated with speech delay, contractures, hypertonia and blepharophimosis
12. Vascular and connective tissue anomalies associated with X-linked periventricular heterotopia due to mutations in Filamin A.
13. Connective tissue spectrum abnormalities associated with spontaneous cerebrospinal fluid leaks: a prospective study.
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.