European Journal of Human Genetics - EMQN Best Practice Guidelines for molecular and haematology methods for carrier identification and prenatal diagnosis of the haemoglobinopathies

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European Journal of Human Genetics - EMQN Best Practice Guidelines for molecular and haematology methods for carrier identification and prenatal diagnosis of the haemoglobinopathies

Genomics in Practice

EMQN best practice guidelines for molecular and haematology methods for carrier identification and prenatal diagnosis of the haemoglobinopathies
Joanne Traeger-Synodinos et al. Eur J Human Genetics, July 23, 2014

Improved molecular diagnosis by the detection of exonic deletions with target gene capture and deep sequencing. 
Yanming Feng et al. Genetics in Medicine, July 17, 2014

Horizontal integration of OMIM across the medical school preclinical curriculum for early reinforcement of clinical genetics principles. 
Adam C. Diehl et al. Genetics in Medicine, July 17, 2014 

Multiplex genetic testing: reconsidering utility and informed consent in the era of next-generation sequencing  
Bradbury AR, et al. Genet Med 2014 Jul

Perceptions of genetic testing and genomic medicine among drug users 
Perlman DC, et al. Int J Drug Policy 2014 Jun

Pharmacogenomic knowledge gaps and educational resource needs among physicians in selected specialties 
Johansen Taber KA & Dickinson BD Pharmgenomics Pers Med 2014;7:145-62

Variant detection sensitivity and biases in whole genome and exome sequencing
Alison M Meynert, et al. BMC Bioinformatics, July 19, 2014

Majority of Americans unaware of personalized medicine: Survey, Genome Web, Jul 22 [by free subscription only]