Hand and fibrillin-1 deposition abnormalities in Loeys-Dietz syndrome-expanding the clinical spectrum-Reference-Cited by-同舟云学术

Hand and fibrillin-1 deposition abnormalities in Loeys-Dietz syndrome-expanding the clinical spectrum

Published:2013-11-05 Issue:2 Volume:164 Page:461-466
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Chung Brian H.Y.¹,Bradley Tim²,Grosse-Wortmann Lars²,Blaser Susan³,Dirks Peter⁴,Hinek Aleksander⁵,Chitayat David⁶⁷

Affiliation:

1. Department of Paediatrics and Adolescent Medicine; Centre for Reproduction, Growth and Development, The University of Hong Kong; Hong Kong Hong Kong

2. Division of Cardiology, The Hospital for Sick Children; University of Toronto; Toronto Ontario Canada

3. Division of Neuroradiology, The Hospital for Sick Children; University of Toronto; Toronto Ontario Canada

4. Division of Neurosurgery, The Hospital for Sick Children; University of Toronto; Toronto Ontario Canada

5. Division of Cardiovascular Research, The Hospital for Sick Children; University of Toronto; Toronto Ontario Canada

6. Division of Clinical and Metabolic Genetics, The Hospital for Sick Children; University of Toronto; Toronto Ontario Canada

7. Mount Sinai Hospital, The Prenatal Diagnosis and Medical Genetics Program; University of Toronto; Toronto Ontario Canada

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.36246/fullpdf

Reference16 articles.

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3. Isolated ductus arteriosus aneurysm in the fetus and infant: A multi-institutional experience;Dyamenahalli;J Am Coll Cardiol,2000

4. Rationale and design of a randomized clinical trial (Marfan Sartan) of angiotensin II receptor blocker therapy versus placebo in individuals with Marfan syndrome;Detaint;Arch Cardiovasc Dis,2010

5. Musculoskeletal findings of Loeys-Dietz syndrome;Erkula;J Bone Joint Surg Am,2010

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