Edition 65 - 2017, September / Subject Review

Subject Review – Ed. 65

Number 65. Subject Review

Taken from:
Horm Res Paediatr, DOI: 10.1159/000464143
May 2017
Horm Res Paediatr. 2017;87(6):412-422.
(See On Line Publication, as well as Spanish translation authorized by Karger AG, 2017 S. Basel)

 

Novel Insights from Clinical Practice
Expanding Genetic and Functional
Diagnoses of IGF1R  Haplo-insufficiencies.

Paula Ocaranza a, Marjorie C. Golekoh b, Shayne F. Andrew c, Michael H. Guo d, Paul Kaplowitz e, Howard Saal f, Ron G. Rosenfeld g, Andrew Dauber C, Fernando Cassorla a, Philippe F. Backeljauw c, Vivian Hwa c.

a Institute of Maternal and Child Research, School of Medicine, University of Chile, Santiago, Chile; b Pediatric Endocrinology, Children’s Hospital of Michigan, Detroit, MI, USA; c Cincinnati Center for Growth Disorders, Division of Endocrinology, Cincinnati Children’s Hospital Medical Center, Cincinnati, OH, USA; d
Division of Endocrinology, Boston Children’s Hospital and Department of Genetics, Harvard Medical School, Boston, MA, USA; e Division of Pediatric Endocrinology and Diabetes, Children’s National Health System, Washington, DC, USA; f Division of Human Genetics, Cincinnati Children’s Hospital Medical Center, Cincinnati, OH, USA; g Department of Pediatrics, Oregon Health & Science University, Portland, OR, USA.


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