| Literature DB >> 28476235 |
Emmanuèle C Délot1, Jeanette C Papp2, David E Sandberg3, Eric Vilain4.
Abstract
Although many next-generation sequencing platforms are being created around the world, implementation is facing multiple hurdles. A strong hurdle to the full adherence of clinical teams to the Disorders of Sex Development Translational Research Network (DSD-TRN) guidelines for standardization of reporting and practice is the current lack of integration of the standardized clinical forms into the various electronic medical records at different sites. Time allocated to research is also limited. In spite of these hurdles, genetic information for half the enrolled patients is already available in the DSD-TRN registry, and early results demonstrate the value of such an infrastructure.Entities:
Keywords: Disorders of sex development; Genomic sequencing; Genotype; Phenotype
Mesh:
Year: 2017 PMID: 28476235 PMCID: PMC5714504 DOI: 10.1016/j.ecl.2017.01.015
Source DB: PubMed Journal: Endocrinol Metab Clin North Am ISSN: 0889-8529 Impact factor: 4.741