Publications by authors named "Meagan Cochran"

5Publications

High Incidence of Noonan Syndrome Features Including Short Stature and Pulmonic Stenosis in Patients carrying NF1 Missense Mutations Affecting p.Arg1809: Genotype-Phenotype Correlation.

Hum Mutat 2015 Nov 21;36(11):1052-63. Epub 2015 Aug 21.

Department of Genetics, Medical Genomics Laboratory, University of Alabama at Birmingham, Birmingham, Alabama.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5049609PMC
http://dx.doi.org/10.1002/humu.22832DOI Listing
November 2015

International adoption of children with birth defects: current knowledge and areas for further research.

Curr Opin Pediatr 2014 Dec;26(6):621-5

Department of Genetics, University of Alabama at Birmingham, Birmingham, Alabama, USA.

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http://content.wkhealth.com/linkback/openurl?sid=WKPTLP:land
Publisher Site
http://dx.doi.org/10.1097/MOP.0000000000000144DOI Listing
December 2014