Adults with genetic syndromes and cardiovascular abnormalities: clinical history and management
Open Access
- 1 July 2008
- journal article
- review article
- Published by Elsevier BV in Genetics in Medicine
- Vol. 10 (7), 469-494
- https://doi.org/10.1097/gim.0b013e3181772111
Abstract
No abstract availableKeywords
This publication has 167 references indexed in Scilit:
- 22q11.2 Distal Deletion: A Recurrent Genomic Disorder Distinct from DiGeorge Syndrome and Velocardiofacial SyndromeAmerican Journal of Human Genetics, 2008
- Long-Term Follow-Up in 12 Children with Pulmonary Arteriovenous Malformations: Confirmation of Hereditary Hemorrhagic Telangiectasia in all CasesThe Journal of Pediatrics, 2007
- Rationale and design of a randomized clinical trial of β-blocker therapy (atenolol) versus angiotensin II receptor blocker therapy (losartan) in individuals with Marfan syndromeAmerican Heart Journal, 2007
- Growth Hormone Treatment and Left Ventricular Dimensions in Turner SyndromeThe Journal of Pediatrics, 2007
- Mutations in the cardiac transcription factor NKX2.5 affect diverse cardiac developmental pathwaysJCI Insight, 1999
- Mutations in human cause limb and cardiac malformation in Holt-Oram syndromeNature Genetics, 1997
- Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene familyNature Genetics, 1997
- Sudden death in Williams syndrome: Report of ten casesThe Journal of Pediatrics, 1996
- lschemic stroke and intracranial multifocal cerebral arteriopathy in Williams syndromeThe Journal of Pediatrics, 1995
- Cerebral artery stenoses in Williams syndrome cause strokes in childhoodThe Journal of Pediatrics, 1995