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Matepair sequencing for the detection of chromosomal aberrations in patients with intellectual disability and congenital malformations

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Chicago
Vergult, Sarah, Ellen Van Binsbergen, TOM SANTE, Silke Nowak, Olivier Vanakker, Kathleen Claes, Bruce Poppe, et al. 2013. “Matepair Sequencing for the Detection of Chromosomal Aberrations in Patients with Intellectual Disability and Congenital Malformations.” In Belgian Society of Human Genetics, 13th Annual Meeting, Abstracts.
APA
Vergult, S., Van Binsbergen, E., SANTE, T., Nowak, S., Vanakker, O., Claes, K., Poppe, B., et al. (2013). Matepair sequencing for the detection of chromosomal aberrations in patients with intellectual disability and congenital malformations. Belgian Society of Human Genetics, 13th Annual meeting, Abstracts. Presented at the 13th Annual meeting of the Belgian Society of Human Genetics (BeSHG).
Vancouver
1.
Vergult S, Van Binsbergen E, SANTE T, Nowak S, Vanakker O, Claes K, et al. Matepair sequencing for the detection of chromosomal aberrations in patients with intellectual disability and congenital malformations. Belgian Society of Human Genetics, 13th Annual meeting, Abstracts. 2013.
MLA
Vergult, Sarah, Ellen Van Binsbergen, TOM SANTE, et al. “Matepair Sequencing for the Detection of Chromosomal Aberrations in Patients with Intellectual Disability and Congenital Malformations.” Belgian Society of Human Genetics, 13th Annual Meeting, Abstracts. 2013. Print.
@inproceedings{6973736,
  author       = {Vergult, Sarah and Van Binsbergen, Ellen and Sante, Tom and Nowak, Silke and Vanakker, Olivier and Claes, Kathleen and Poppe, Bruce and Van der Aa, Nathalie and Van Roosmalen, MJ and Duran, K and Tavakoli-Yaraki, M and Swinkels, M and van den Boomgaard, MJ and van Haelst, M and Roelens, Filip and Speleman, Franki and Cuppen, Edwin and Mortier, Geert and Menten, Bj{\"o}rn},
  booktitle    = {Belgian Society of Human Genetics, 13th Annual meeting, Abstracts},
  language     = {eng},
  location     = {Brussels, Belgium},
  title        = {Matepair sequencing for the detection of chromosomal aberrations in patients with intellectual disability and congenital malformations},
  year         = {2013},
}