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Recurrent duplications of 17q12 associated with variable phenotypes

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duplication, genotype phenotype, AUTISM SPECTRUM DISORDER, GENOMIC REARRANGEMENTS, CNV, DISCOVERY, EPILEPSY, RENAL-DISEASE, DEVELOPMENTAL DELAY, PATIENT, TCF2 GENE, MICRODUPLICATION, ESOPHAGEAL ATRESIA

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Chicago
Mitchell, Elyse, Andrew Douglas, Susanne Kjaegaard, Bert Callewaert, ARNAUD VANLANDER, Sandra Janssens, Amy Lawson Yuen, et al. 2015. “Recurrent Duplications of 17q12 Associated with Variable Phenotypes.” American Journal of Medical Genetics Part A 167 (12): 3038–3045.
APA
Mitchell, E., Douglas, A., Kjaegaard, S., Callewaert, B., VANLANDER, A., Janssens, S., Yuen, A. L., et al. (2015). Recurrent duplications of 17q12 associated with variable phenotypes. AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 167(12), 3038–3045.
Vancouver
1.
Mitchell E, Douglas A, Kjaegaard S, Callewaert B, VANLANDER A, Janssens S, et al. Recurrent duplications of 17q12 associated with variable phenotypes. AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 2015;167(12):3038–45.
MLA
Mitchell, Elyse, Andrew Douglas, Susanne Kjaegaard, et al. “Recurrent Duplications of 17q12 Associated with Variable Phenotypes.” AMERICAN JOURNAL OF MEDICAL GENETICS PART A 167.12 (2015): 3038–3045. Print.
@article{7083778,
  author       = {Mitchell, Elyse and Douglas, Andrew and Kjaegaard, Susanne and Callewaert, Bert and Vanlander, Arnaud and Janssens, Sandra and Yuen, Amy Lawson and Skinner, Cindy and Failla, Pinella and Alberti, Antonino and Avola, Emanuela and Fichera, Marco and Kibaek, Maria and Digilio, Maria C and Hannibal, Mark C and den Hollander, Nicolette S and Bizzarri, Veronica and Renieri, Alessandra and Mencarelli, Maria Antonietta and Fitzgerald, Tomas and Piazzolla, Serena and van Oudenhove, Elke and Romano, Corrado and Schwartz, Charles and Eichler, Evan E and Slavotinek, Anne and Escobar, Luis and Rajan, Diana and Crolla, John and Carter, Nigel and Hodge, Jennelle C and Mefford, Heather C},
  issn         = {1552-4825},
  journal      = {AMERICAN JOURNAL OF MEDICAL GENETICS PART A},
  keyword      = {duplication,genotype phenotype,AUTISM SPECTRUM DISORDER,GENOMIC REARRANGEMENTS,CNV,DISCOVERY,EPILEPSY,RENAL-DISEASE,DEVELOPMENTAL DELAY,PATIENT,TCF2 GENE,MICRODUPLICATION,ESOPHAGEAL ATRESIA},
  language     = {eng},
  number       = {12},
  pages        = {3038--3045},
  title        = {Recurrent duplications of 17q12 associated with variable phenotypes},
  url          = {http://dx.doi.org/10.1002/ajmg.a.37351},
  volume       = {167},
  year         = {2015},
}

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