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Recurrent duplications of 17q12 associated with variable phenotypes

Elyse Mitchell, Andrew Douglas, Susanne Kjaegaard, Bert Callewaert UGent, Arnaud Vanlander, Sandra Janssens, Amy Lawson Yuen, Cindy Skinner, Pinella Failla, Antonino Alberti, et al. (2015) AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 167(12). p.3038-3045
Please use this url to cite or link to this publication:
author
organization
year
type
journalArticle (original)
publication status
published
subject
keyword
duplication, genotype phenotype, AUTISM SPECTRUM DISORDER, GENOMIC REARRANGEMENTS, CNV, DISCOVERY, EPILEPSY, RENAL-DISEASE, DEVELOPMENTAL DELAY, PATIENT, TCF2 GENE, MICRODUPLICATION, ESOPHAGEAL ATRESIA
journal title
AMERICAN JOURNAL OF MEDICAL GENETICS PART A
Am. J. Med. Genet. A
volume
167
issue
12
pages
3038 - 3045
Web of Science type
Article
Web of Science id
000367668600020
JCR category
GENETICS & HEREDITY
JCR impact factor
2.082 (2015)
JCR rank
106/165 (2015)
JCR quartile
3 (2015)
ISSN
1552-4825
DOI
10.1002/ajmg.a.37351
language
English
UGent publication?
yes
classification
A1
copyright statement
I have transferred the copyright for this publication to the publisher
id
7083778
handle
http://hdl.handle.net/1854/LU-7083778
date created
2016-02-12 13:36:42
date last changed
2016-12-19 15:47:11
@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},
}

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.