Skip to main navigation
Skip to search
Skip to main content
WashU Medicine Research Profiles Home
Help & FAQ
Link opens in a new tab
Search content at WashU Medicine Research Profiles
Home
Profiles
Departments, Divisions and Centers
Research output
Genotype–phenotype correlations in children with hht
the Brain Vascular Malformation Consortium HHT Investigator Group
Division of Rheumatology
Institute of Clinical and Translational Sciences (ICTS)
Division of Pulmonary & Critical Care Medicine
Research output
:
Contribution to journal
›
Article
›
peer-review
25
Link opens in a new tab
Scopus citations
Overview
Fingerprint
Fingerprint
Dive into the research topics of 'Genotype–phenotype correlations in children with hht'. Together they form a unique fingerprint.
Sort by
Weight
Alphabetically
Keyphrases
Hereditary Hemorrhagic Telangiectasia
100%
Genotype-phenotype Correlation
100%
Pulmonary Arteriovenous Malformation
50%
Brain Vascular Malformation
50%
Pediatric
33%
SMAD4
33%
Genotype
33%
Lung
16%
Liver
16%
Central Nervous System
16%
Pediatric Patients
16%
Clinical Data
16%
Gastrointestinal Bleeding
16%
Demographic Data
16%
Genetic Data
16%
Chi-square Test
16%
Arteriovenous Malformation
16%
Vascular Malformation
16%
ALK1
16%
Autosomal Dominant Disorder
16%
Mucocutaneous Telangiectasia
16%
Medicine and Dentistry
Hereditary Hemorrhagic Telangiectasia
100%
Electronystagmography
66%
Pulmonary Arteriovenous Fistula
50%
Cerebrovascular Malformation
50%
Pediatrics
33%
Prevalence
16%
Pediatrics Patient
16%
Gastrointestinal Bleeding
16%
Central Nervous System
16%
Telangiectasia
16%
Autosomal Dominant Inheritance
16%
Chi Square Test
16%
Arteriovenous Malformation
16%
Vascular Anomaly
16%
Lung
16%
Diseases
16%
Biochemistry, Genetics and Molecular Biology
Genotyping
100%
Genetics
50%
Autosomal Dominant Inheritance
50%
Prevalence
50%
ACVRL1
50%
Chi-Square Testing
50%
Pharmacology, Toxicology and Pharmaceutical Science
Rendu Osler Weber Disease
100%
Pulmonary Arteriovenous Fistula
50%
Cerebrovascular Malformation
50%
Prevalence
16%
Gastrointestinal Hemorrhage
16%
Congenital Blood Vessel Malformation
16%
Telangiectasia
16%
Arteriovenous Malformation
16%
Diseases
16%
Immunology and Microbiology
Prevalence
100%
Autosomal Dominant Inheritance
100%
Central Nervous System
100%