Developments in our understanding of the genetic basis of birth defects-Reference-Cited by-同舟云学术

Developments in our understanding of the genetic basis of birth defects

Published:2015-05-28 Issue:8 Volume:103 Page:680-691
ISSN:1542-0752
Container-title:Birth Defects Research Part A: Clinical and Molecular Teratology
language:en
Short-container-title:Birth Defects Research Part A: Clinical and Molecular Teratology

Author:

Webber Daniel M.¹,MacLeod Stewart L.¹,Bamshad Michael J.²,Shaw Gary M.³,Finnell Richard H.⁴,Shete Sanjay S.⁵,Witte John S.⁶,Erickson Stephen W.⁷,Murphy Linda D.¹,Hobbs Charlotte¹

Affiliation:

1. Division of Birth Defects Research, Department of Pediatrics; College of Medicine, University of Arkansas for Medical Sciences; Little Rock Arkansas

2. Division of Genetic Medicine, Department of Pediatrics; University of Washington; Seattle Washington

3. Stanford University School of Medicine; Stanford California

4. Dell Pediatric Research Institute, Department of Nutritional Sciences; The University of Texas at Austin; Austin Texas

5. Department of Epidemiology; MD Anderson Cancer Center; Houston Texas

6. Department of Epidemiology and Biostatistics; University of California San Francisco; San Francisco California

7. Department of Biostatistics; College of Medicine, University of Arkansas for Medical Sciences; Little Rock Arkansas

Funder

National Institute of Child Health and Human Development

National Center on Birth Defects and Developmental Disabilities

Publisher

Wiley

Subject

Developmental Biology,Embryology,General Medicine,Pediatrics, Perinatology, and Child Health

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/bdra.23385/fullpdf

Reference104 articles.

1. An integrated map of genetic variation from 1,092 human genomes;1000 Genomes Project Consortium;Nature,2012

2. Genome structural variation discovery and genotyping;Alkan;Nat Rev Genet,2011

3. Association of genetic variation of the transforming growth factor-alpha gene with cleft lip and palate;Ardinger;Am J Hum Genet,1989

4. Exome analysis of a family with pleiotropic congenital heart disease;Arrington;Circ Cardiovasc Genet,2012

5. Rapid DNA methylation changes after exposure to traffic particles;Baccarelli;Am J Respir Crit Care Med,2009

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