Carney complex and McCune Albright syndrome: An overview of clinical manifestations and human molecular genetics-Reference-Cited by-同舟云学术

Carney complex and McCune Albright syndrome: An overview of clinical manifestations and human molecular genetics

Published:2014-04 Issue:1-2 Volume:386 Page:85-91
ISSN:0303-7207
Container-title:Molecular and Cellular Endocrinology
language:en
Short-container-title:Molecular and Cellular Endocrinology

Author:

Salpea Paraskevi,Stratakis Constantine A.

Publisher

Elsevier BV

Subject

Endocrinology,Molecular Biology,Biochemistry

Reference92 articles.

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3. A large family with Carney complex caused by the S147G PRKAR1A mutation shows a unique spectrum of disease including adrenocortical cancer;Anselmo;J. Clin. Endocrinol. Metab.,2012

4. Peutz–Jeghers syndrome: a systematic review and recommendations for management;Beggs;Gut,2010

5. The cyclic adenosine 3′,5′-monophosphate-responsive factor CREB is constitutively activated in human somatotroph adenomas;Bertherat;Mol. Endocrinol.,1995

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