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Y RIN2 syndrome : expanding the clinical phenotype

Simonetta Rosato, Delfien Syx UGent, Ivan Ivanovski, Marzia Pollazzon, Daniela Santodirocco, Loredana De Marco, Marina Beltrami, Bert Callewaert UGent, Livia Garavelli and Fransiska Malfait UGent (2016) AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 170(9). p.2408-2415
Please use this url to cite or link to this publication:
author
organization
year
type
journalArticle (original)
publication status
published
subject
keyword
ENDOTHELIAL-CELL ADHESION, MACS SYNDROME, ENDOCYTOSIS, RAB5, RIN2, scoliosis, progressive facial coarsening, skin hyperextensibility, cutis laxa, sparse hair
journal title
AMERICAN JOURNAL OF MEDICAL GENETICS PART A
Am. J. Med. Genet. A
volume
170
issue
9
pages
2408 - 2415
Web of Science type
Article
Web of Science id
000383608700026
JCR category
GENETICS & HEREDITY
JCR impact factor
2.259 (2016)
JCR rank
96/166 (2016)
JCR quartile
3 (2016)
ISSN
1552-4825
1552-4833
DOI
10.1002/ajmg.a.37789
language
English
UGent publication?
yes
classification
A1
copyright statement
I have transferred the copyright for this publication to the publisher
id
8510226
handle
http://hdl.handle.net/1854/LU-8510226
date created
2017-02-20 11:05:10
date last changed
2017-02-20 13:06:00
@article{8510226,
  author       = {Rosato, Simonetta and Syx, Delfien and Ivanovski, Ivan and Pollazzon, Marzia and Santodirocco, Daniela and De Marco, Loredana and Beltrami, Marina and Callewaert, Bert and Garavelli, Livia and Malfait, Fransiska},
  issn         = {1552-4825},
  journal      = {AMERICAN JOURNAL OF MEDICAL GENETICS PART A},
  keyword      = {ENDOTHELIAL-CELL ADHESION,MACS SYNDROME,ENDOCYTOSIS,RAB5,RIN2,scoliosis,progressive facial coarsening,skin hyperextensibility,cutis laxa,sparse hair},
  language     = {eng},
  number       = {9},
  pages        = {2408--2415},
  title        = {Y RIN2 syndrome : expanding the clinical phenotype},
  url          = {http://dx.doi.org/10.1002/ajmg.a.37789},
  volume       = {170},
  year         = {2016},
}

Chicago
Rosato, Simonetta, Delfien Syx, Ivan Ivanovski, Marzia Pollazzon, Daniela Santodirocco, Loredana De Marco, Marina Beltrami, Bert Callewaert, Livia Garavelli, and Fransiska Malfait. 2016. “Y RIN2 Syndrome : Expanding the Clinical Phenotype.” American Journal of Medical Genetics Part A 170 (9): 2408–2415.
APA
Rosato, S., Syx, D., Ivanovski, I., Pollazzon, M., Santodirocco, D., De Marco, L., Beltrami, M., et al. (2016). Y RIN2 syndrome : expanding the clinical phenotype. AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 170(9), 2408–2415.
Vancouver
1.
Rosato S, Syx D, Ivanovski I, Pollazzon M, Santodirocco D, De Marco L, et al. Y RIN2 syndrome : expanding the clinical phenotype. AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 2016;170(9):2408–15.
MLA
Rosato, Simonetta, Delfien Syx, Ivan Ivanovski, et al. “Y RIN2 Syndrome : Expanding the Clinical Phenotype.” AMERICAN JOURNAL OF MEDICAL GENETICS PART A 170.9 (2016): 2408–2415. Print.