Utility of Whole Genome Sequencing for Detection of Newborn Screening Disorders in a Population Cohort of ∼1700 Neonates

Autor:	Ramaswamy K. Iyer, Stauffer Daniel, Alex Yashchenko, Robin Baker, Aaron Black, Amber D. Gaither, Alina Khromykh, Dale L. Bodian, Elisabeth Klein, Rajiv Baveja, Benjamin D. Solomon, John E. Niederhuber, Greg Eley, Joseph G. Vockley, Irina Remsburg, Radhika Hastak, Kathi Huddleston
Rok vydání:	2016
Předmět:	Whole genome sequencing Newborn screening Pediatrics medicine.medical_specialty business.industry Pediatrics Perinatology and Child Health Medicine Population cohort business
Zdroj:	Pediatrics. 137:492A-492A
ISSN:	1098-4275 0031-4005
DOI:	10.1542/peds.137.supplement_3.492a
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::24aec4fc8bb5c85ea4ba798fd862fdbf https://doi.org/10.1542/peds.137.supplement_3.492a Zobrazit plný text záznamu