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ENDOTHELIAL-CELL ADHESION, MACS SYNDROME, ENDOCYTOSIS, RAB5, RIN2, scoliosis, progressive facial coarsening, skin hyperextensibility, cutis laxa, sparse hair

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Citation

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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.
@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},
}

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