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The diagnostic value of next generation sequencing in familial nonsyndromic congenital heart defects

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OUTLET RIGHT VENTRICLE, congenital heart defects, ZIC3 MUTATIONS, GENE, TETRALOGY, DISEASE, HOLT-ORAM-SYNDROME, SUPRAVALVULAR AORTIC-STENOSIS, FUNCTIONAL-ANALYSIS, massive parallel sequencing, GREAT-ARTERIES, TBX5 MUTATIONS, genetic testing

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MLA
Jia, Yaojuan, et al. “The Diagnostic Value of next Generation Sequencing in Familial Nonsyndromic Congenital Heart Defects.” AMERICAN JOURNAL OF MEDICAL GENETICS PART A, vol. 167, no. 8, 2015, pp. 1822–29, doi:10.1002/ajmg.a.37108.
APA
Jia, Y., Louw, J. J., Breckpot, J., Callewaert, B., Barrea, C., Sznajer, Y., … Corveleyn, A. (2015). The diagnostic value of next generation sequencing in familial nonsyndromic congenital heart defects. AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 167(8), 1822–1829. https://doi.org/10.1002/ajmg.a.37108
Chicago author-date
Jia, Yaojuan, Jacoba J Louw, Jeroen Breckpot, Bert Callewaert, Catherine Barrea, Yves Sznajer, Marc Gewillig, et al. 2015. “The Diagnostic Value of next Generation Sequencing in Familial Nonsyndromic Congenital Heart Defects.” AMERICAN JOURNAL OF MEDICAL GENETICS PART A 167 (8): 1822–29. https://doi.org/10.1002/ajmg.a.37108.
Chicago author-date (all authors)
Jia, Yaojuan, Jacoba J Louw, Jeroen Breckpot, Bert Callewaert, Catherine Barrea, Yves Sznajer, Marc Gewillig, Erika Souche, Luc Dehaspe, Joris Robert Vermeesch, Diether Lambrechts, Koenraad Devriendt, and Anniek Corveleyn. 2015. “The Diagnostic Value of next Generation Sequencing in Familial Nonsyndromic Congenital Heart Defects.” AMERICAN JOURNAL OF MEDICAL GENETICS PART A 167 (8): 1822–1829. doi:10.1002/ajmg.a.37108.
Vancouver
1.
Jia Y, Louw JJ, Breckpot J, Callewaert B, Barrea C, Sznajer Y, et al. The diagnostic value of next generation sequencing in familial nonsyndromic congenital heart defects. AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 2015;167(8):1822–9.
IEEE
[1]
Y. Jia et al., “The diagnostic value of next generation sequencing in familial nonsyndromic congenital heart defects,” AMERICAN JOURNAL OF MEDICAL GENETICS PART A, vol. 167, no. 8, pp. 1822–1829, 2015.
@article{6922238,
  author       = {{Jia, Yaojuan and Louw, Jacoba J and Breckpot, Jeroen and Callewaert, Bert and Barrea, Catherine and Sznajer, Yves and Gewillig, Marc and Souche, Erika and Dehaspe, Luc and Vermeesch, Joris Robert and Lambrechts, Diether and Devriendt, Koenraad and Corveleyn, Anniek}},
  issn         = {{1552-4825}},
  journal      = {{AMERICAN JOURNAL OF MEDICAL GENETICS PART A}},
  keywords     = {{OUTLET RIGHT VENTRICLE,congenital heart defects,ZIC3 MUTATIONS,GENE,TETRALOGY,DISEASE,HOLT-ORAM-SYNDROME,SUPRAVALVULAR AORTIC-STENOSIS,FUNCTIONAL-ANALYSIS,massive parallel sequencing,GREAT-ARTERIES,TBX5 MUTATIONS,genetic testing}},
  language     = {{eng}},
  number       = {{8}},
  pages        = {{1822--1829}},
  title        = {{The diagnostic value of next generation sequencing in familial nonsyndromic congenital heart defects}},
  url          = {{http://doi.org/10.1002/ajmg.a.37108}},
  volume       = {{167}},
  year         = {{2015}},
}

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