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Implementation of genomic arrays in prenatal diagnosis: the Belgian approach to meet the challenges

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Keywords
Variant of unknown significance, Copy number variant, Guidelines, Prenatal diagnosis, Prenatal microarray, Incidental finding, COPY NUMBER VARIATION, CHROMOSOMAL MICROARRAY, DEVELOPMENTAL DELAY, CGH, VARIANTS, 17Q12, GENE

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MLA
Vanakker, Olivier, Catheline Vilain, Katrien Janssens, et al. “Implementation of Genomic Arrays in Prenatal Diagnosis: The Belgian Approach to Meet the Challenges.” EUROPEAN JOURNAL OF MEDICAL GENETICS 57.4 (2014): 151–156. Print.
APA
Vanakker, O., Vilain, C., Janssens, K., Van der Aa, N., Smits, G., Bandelier, C., Blaumeiser, B., et al. (2014). Implementation of genomic arrays in prenatal diagnosis: the Belgian approach to meet the challenges. EUROPEAN JOURNAL OF MEDICAL GENETICS, 57(4), 151–156.
Chicago author-date
Vanakker, Olivier, Catheline Vilain, Katrien Janssens, Nathalie Van der Aa, Guillaume Smits, Claude Bandelier, Bettina Blaumeiser, et al. 2014. “Implementation of Genomic Arrays in Prenatal Diagnosis: The Belgian Approach to Meet the Challenges.” European Journal of Medical Genetics 57 (4): 151–156.
Chicago author-date (all authors)
Vanakker, Olivier, Catheline Vilain, Katrien Janssens, Nathalie Van der Aa, Guillaume Smits, Claude Bandelier, Bettina Blaumeiser, Saskia Bulk, Jean-Hubert Caberg, Anne De Leener, Marjan De Rademaeker, Thomy de Ravel, Julie Desir, Anne Destree, Annelies Dheedene, Stéphane Gaillez, Bernard Grisart, Ann-Céline Hellin, Sandra Janssens, Kathelijn Keymolen, Björn Menten, Bruno Pichon, Marie Ravoet, Nicole Revencu, Sonia Rombout, Catherine Staessens, Ann Van Den Bogaert, Kris Van Den Bogaert, Joris R Vermeesch, Frank Kooy, Yves Sznajer, and Koen Devriendt. 2014. “Implementation of Genomic Arrays in Prenatal Diagnosis: The Belgian Approach to Meet the Challenges.” European Journal of Medical Genetics 57 (4): 151–156.
Vancouver
1.
Vanakker O, Vilain C, Janssens K, Van der Aa N, Smits G, Bandelier C, et al. Implementation of genomic arrays in prenatal diagnosis: the Belgian approach to meet the challenges. EUROPEAN JOURNAL OF MEDICAL GENETICS. 2014;57(4):151–6.
IEEE
[1]
O. Vanakker et al., “Implementation of genomic arrays in prenatal diagnosis: the Belgian approach to meet the challenges,” EUROPEAN JOURNAL OF MEDICAL GENETICS, vol. 57, no. 4, pp. 151–156, 2014.
@article{4342254,
  author       = {Vanakker, Olivier and Vilain, Catheline and Janssens, Katrien and Van der Aa, Nathalie and Smits, Guillaume and Bandelier, Claude and Blaumeiser, Bettina and Bulk, Saskia and Caberg, Jean-Hubert and De Leener, Anne and De Rademaeker, Marjan and de Ravel, Thomy and Desir, Julie and Destree, Anne and Dheedene, Annelies and Gaillez, Stéphane and Grisart, Bernard and Hellin, Ann-Céline and Janssens, Sandra and Keymolen, Kathelijn and Menten, Björn and Pichon, Bruno and Ravoet, Marie and Revencu, Nicole and Rombout, Sonia and Staessens, Catherine and Van Den Bogaert, Ann and Van Den Bogaert, Kris and Vermeesch, Joris R and Kooy, Frank and Sznajer, Yves and Devriendt, Koen},
  issn         = {1769-7212},
  journal      = {EUROPEAN JOURNAL OF MEDICAL GENETICS},
  keywords     = {Variant of unknown significance,Copy number variant,Guidelines,Prenatal diagnosis,Prenatal microarray,Incidental finding,COPY NUMBER VARIATION,CHROMOSOMAL MICROARRAY,DEVELOPMENTAL DELAY,CGH,VARIANTS,17Q12,GENE},
  language     = {eng},
  number       = {4},
  pages        = {151--156},
  title        = {Implementation of genomic arrays in prenatal diagnosis: the Belgian approach to meet the challenges},
  url          = {http://dx.doi.org/10.1016/j.ejmg.2014.02.002},
  volume       = {57},
  year         = {2014},
}

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