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Clinical utility gene card for: Marfan syndrome type 1 and related phenotypes [FBN1]

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DISORDERS, RECURRENCE, TGFBR2 MUTATIONS, I FIBRILLINOPATHIES, DIAGNOSTIC-CRITERIA, MOSAICISM, 1009 PROBANDS, FEATURES, ECTOPIA LENTIS, IDENTIFICATION

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Chicago
Arslan-Kirchner, Mine, Eloisa Arbustini, Catherine Boileau, Anne Child, Gwenaelle Collod-Beroud, Anne De Paepe, Jörg Epplen, Guillaume Jondeau, Bart Loeys, and Laurence Faivre. 2010. “Clinical Utility Gene Card for: Marfan Syndrome Type 1 and Related Phenotypes [FBN1].” European Journal of Human Genetics.
APA
Arslan-Kirchner, M., Arbustini, E., Boileau, C., Child, A., Collod-Beroud, G., De Paepe, A., Epplen, J., et al. (2010). Clinical utility gene card for: Marfan syndrome type 1 and related phenotypes [FBN1]. EUROPEAN JOURNAL OF HUMAN GENETICS.
Vancouver
1.
Arslan-Kirchner M, Arbustini E, Boileau C, Child A, Collod-Beroud G, De Paepe A, et al. Clinical utility gene card for: Marfan syndrome type 1 and related phenotypes [FBN1]. EUROPEAN JOURNAL OF HUMAN GENETICS. 2010.
MLA
Arslan-Kirchner, Mine, Eloisa Arbustini, Catherine Boileau, et al. “Clinical Utility Gene Card for: Marfan Syndrome Type 1 and Related Phenotypes [FBN1].” EUROPEAN JOURNAL OF HUMAN GENETICS 2010 : n. pag. Print.
@misc{1064550,
  author       = {Arslan-Kirchner, Mine and Arbustini, Eloisa and Boileau, Catherine and Child, Anne and Collod-Beroud, Gwenaelle and De Paepe, Anne and Epplen, J{\"o}rg and Jondeau, Guillaume and Loeys, Bart and Faivre, Laurence},
  issn         = {1018-4813},
  keyword      = {DISORDERS,RECURRENCE,TGFBR2 MUTATIONS,I FIBRILLINOPATHIES,DIAGNOSTIC-CRITERIA,MOSAICISM,1009 PROBANDS,FEATURES,ECTOPIA LENTIS,IDENTIFICATION},
  language     = {eng},
  number       = {9},
  pages        = {4},
  series       = {EUROPEAN JOURNAL OF HUMAN GENETICS},
  title        = {Clinical utility gene card for: Marfan syndrome type 1 and related phenotypes [FBN1]},
  url          = {http://dx.doi.org/10.1038/ejhg.2010.42},
  volume       = {18},
  year         = {2010},
}

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