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Extending the phenotype of recurrent rearrangements of 16p11.2: deletions in mentally retarded patients without autism and in normal individuals

EK Bijlsma, ACJ Gijsbers, JHM Schuurs-Hoeijmakers, A van Haeringen, DEF van de Putte, BM Anderlid, J Lundin, P Lapunzina, LAP Jurado and BARBARA DELLE CHIAIE UGent, et al. (2009) EUROPEAN JOURNAL OF MEDICAL GENETICS. 52(2-3). p.77-87
Please use this url to cite or link to this publication:
author
organization
year
type
journalArticle (original)
publication status
published
subject
keyword
MICRODELETION, MICRODUPLICATION 22Q11.2, Variable phenotype, Microdeletion syndrome, Chromosome 16p11.2, DISCOVERY, DISORDERS, MICROARRAYS, RETARDATION, LEUKEMIA, POLYMORPHISM
journal title
EUROPEAN JOURNAL OF MEDICAL GENETICS
Eur. J. Med. Genet.
volume
52
issue
2-3
pages
11 pages
Web of Science type
Article
Web of Science id
000266903500002
JCR category
GENETICS & HEREDITY
JCR impact factor
1.568 (2009)
JCR rank
106/142 (2009)
JCR quartile
3 (2009)
ISSN
1769-7212
DOI
10.1016/j.ejmg.2009.03.006
language
English
UGent publication?
yes
classification
A1
copyright statement
I have transferred the copyright for this publication to the publisher
id
856878
handle
http://hdl.handle.net/1854/LU-856878
date created
2010-02-09 14:39:22
date last changed
2015-06-17 11:21:25
@article{856878,
  author       = {Bijlsma, EK and Gijsbers, ACJ and Schuurs-Hoeijmakers, JHM and van Haeringen, A and van de Putte, DEF and Anderlid, BM and Lundin, J and Lapunzina, P and Jurado, LAP and DELLE CHIAIE, BARBARA and Loeys, Bart and Menten, Bj{\"o}rn and Oostra, Ann and VERHELST, HELENE and Amor, DJ and Bruno, DL and van Essen, AJ and Hordijk, R and Sikkema-Raddatz, B and Verbruggen, KT and Jongmans, MCJ and Pfundt, R and Reeser, HM and Breuning, MH and Ruivenkamp, CAL},
  issn         = {1769-7212},
  journal      = {EUROPEAN JOURNAL OF MEDICAL GENETICS},
  keyword      = {MICRODELETION,MICRODUPLICATION 22Q11.2,Variable phenotype,Microdeletion syndrome,Chromosome 16p11.2,DISCOVERY,DISORDERS,MICROARRAYS,RETARDATION,LEUKEMIA,POLYMORPHISM},
  language     = {eng},
  number       = {2-3},
  pages        = {77--87},
  title        = {Extending the phenotype of recurrent rearrangements of 16p11.2: deletions in mentally retarded patients without autism and in normal individuals},
  url          = {http://dx.doi.org/10.1016/j.ejmg.2009.03.006},
  volume       = {52},
  year         = {2009},
}

Chicago
Bijlsma, EK, ACJ Gijsbers, JHM Schuurs-Hoeijmakers, A van Haeringen, DEF van de Putte, BM Anderlid, J Lundin, et al. 2009. “Extending the Phenotype of Recurrent Rearrangements of 16p11.2: Deletions in Mentally Retarded Patients Without Autism and in Normal Individuals.” European Journal of Medical Genetics 52 (2-3): 77–87.
APA
Bijlsma, E., Gijsbers, A., Schuurs-Hoeijmakers, J., van Haeringen, A., van de Putte, D., Anderlid, B., Lundin, J., et al. (2009). Extending the phenotype of recurrent rearrangements of 16p11.2: deletions in mentally retarded patients without autism and in normal individuals. EUROPEAN JOURNAL OF MEDICAL GENETICS, 52(2-3), 77–87.
Vancouver
1.
Bijlsma E, Gijsbers A, Schuurs-Hoeijmakers J, van Haeringen A, van de Putte D, Anderlid B, et al. Extending the phenotype of recurrent rearrangements of 16p11.2: deletions in mentally retarded patients without autism and in normal individuals. EUROPEAN JOURNAL OF MEDICAL GENETICS. 2009;52(2-3):77–87.
MLA
Bijlsma, EK, ACJ Gijsbers, JHM Schuurs-Hoeijmakers, et al. “Extending the Phenotype of Recurrent Rearrangements of 16p11.2: Deletions in Mentally Retarded Patients Without Autism and in Normal Individuals.” EUROPEAN JOURNAL OF MEDICAL GENETICS 52.2-3 (2009): 77–87. Print.