Related references
Note: Only part of the references are listed.Spontaneous Coronary Artery Dissection Insights on Rare Genetic Variation From Genome Sequencing
Keren J. Carss et al.
CIRCULATION-GENOMIC AND PRECISION MEDICINE (2020)
Underdiagnosis of Hereditary Breast Cancer: Are Genetic Testing Guidelines a Tool or an Obstacle?
Peter D. Beitsch et al.
JOURNAL OF CLINICAL ONCOLOGY (2019)
Results of next-generation sequencing gene panel diagnostics including copy-number variation analysis in 810 patients suspected of heritable thoracic aortic disorders
Eline Overwater et al.
HUMAN MUTATION (2018)
Diagnosis, natural history, and management in vascular Ehlers-Danlos syndrome
Peter H. Byers et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS (2017)
The 2017 International Classification of the Ehlers-Danlos Syndromes
Fransiska Malfait et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS (2017)
Spontaneous coronary artery dissection and its association with heritable connective tissue disorders
Stanislav Henkin et al.
HEART (2016)
Spontaneous coronary artery dissection
Christian J. M. Vrints
HEART (2010)
Effect of celiprolol on prevention of cardiovascular events in vascular Ehlers-Danlos syndrome: a prospective randomised, open, blinded-endpoints trial
Kim-Thanh Ong et al.
LANCET (2010)