Applying deep DNA sequencing to common, complex pediatric traits

Letter/Communication

Open access

John M Dagle and Jeffrey C Murray

Pediatrics (Evanston), Vol.130(6), pp.e1677-e1678

12/2012

DOI: 10.1542/peds.2012-2870

PMCID: PMC3507258

PMID: 23166345

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https://doi.org/10.1542/peds.2012-2870View

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Commentary

Mutation

Respiratory Distress Syndrome, Newborn - genetics

Genetic Predisposition to Disease - genetics

ATP-Binding Cassette Transporters - genetics

Humans

Title: Subtitle: Applying deep DNA sequencing to common, complex pediatric traits
Creators: John M Dagle - Department of Pediatrics, University of Iowa, Iowa City, IA 52242, USA
Jeffrey C Murray
Resource Type: Letter/Communication
Publication Details: Pediatrics (Evanston), Vol.130(6), pp.e1677-e1678
DOI: 10.1542/peds.2012-2870
PMID: 23166345
PMCID: PMC3507258
NLM abbreviation: Pediatrics
ISSN: 0031-4005
eISSN: 1098-4275
Publisher: American Academy of Pediatrics; United States
Grant note: R01 HL109199 / NHLBI NIH HHS
Language: English
Date published: 12/2012
Academic Unit: Anatomy and Cell Biology; Stead Family Department of Pediatrics; Epidemiology; Pediatric Dentistry; Craniofacial Anomalies Research Center; Biochemistry and Molecular Biology; Dental Research; Neonatology
Record Identifier: 9984024408302771

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