A Recurrent PDGFRB Mutation Causes Familial Infantile Myofibromatosis-Reference-Cited by-同舟云学术

A Recurrent PDGFRB Mutation Causes Familial Infantile Myofibromatosis

Published:2013-06 Issue:6 Volume:92 Page:996-1000
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Cheung Yee Him,Gayden Tenzin,Campeau Philippe M.,LeDuc Charles A.,Russo Donna,Nguyen Van-Hung,Guo Jiancheng,Qi Ming,Guan Yanfang,Albrecht Steffen,Moroz Brenda,Eldin Karen W.,Lu James T.,Schwartzentruber Jeremy,Malkin David,Berghuis Albert M.,Emil Sherif,Gibbs Richard A.,Burk David L.,Vanstone Megan,Lee Brendan H.,Orchard David,Boycott Kym M.,Chung Wendy K.,Jabado Nada

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference30 articles.

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3. Infantile myofibromatosis. Evidence for an autosomal-dominant disorder;Jennings;Am. J. Surg. Pathol.,1984

4. Autosomal dominant inheritance of infantile myofibromatosis;Zand;Am. J. Med. Genet. A.,2004

5. Infantile myofibromatosis;Chung;Cancer,1981

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