Singleton-Merten syndrome: An autosomal dominant disorder with variable expression-Reference-Cited by-同舟云学术

Singleton-Merten syndrome: An autosomal dominant disorder with variable expression

Published:2013-01-15 Issue:2 Volume:161 Page:360-370
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Feigenbaum Annette,Müller Christine,Yale Christopher,Kleinheinz Johannes,Jezewski Peter,Kehl Hans Gerd,MacDougall Mary,Rutsch Frank,Hennekam Raoul C.M.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.35732/fullpdf

Reference12 articles.

1. Singleton-Merten (S-M) syndrome: Autosomal dominant transmission with variable expression;Feigenbaum;Am J Hum Genet,1988

2. A syndrome of widened medullary cavities of bone, aortic calcification, abnormal dentition, and muscular weakness (The Singleton-Merton syndrome);Gay;Radiology,1976

3. Ascending aortic calcification and calcific aortic stenosis in a young woman;Goldbaum;Am Heart J,1986

4. Idiopathic calcification of the ascending aorta and aortic arch in two young women;McLoughlin;Br Heart J,1974

5. Idiopathic aortitis with calcification of ascending aorta and aortic and mitral valves;Rose;Br Heart J,1976

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