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Comprehensive clinical and molecular assessment of 32 probands with congenital contractural arachnodactyly: report of 14 novel mutations and review of the literature

(2009) HUMAN MUTATION. 30(3). p.334-341
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Organization
Keywords
MICE, FAMILY, MICROFIBRILS, BEALS-SYNDROME, FIBRILLIN-2, GENE, FBN2 MUTATIONS, congenital contractural arachnodactyly, CCA, FBN2, fibrillin 2, genotype-phenotype, MARFAN-SYNDROME

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Citation

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MLA
Callewaert, Bert et al. “Comprehensive Clinical and Molecular Assessment of 32 Probands with Congenital Contractural Arachnodactyly: Report of 14 Novel Mutations and Review of the Literature.” HUMAN MUTATION 30.3 (2009): 334–341. Print.
APA
Callewaert, B., Loeys, B., Ficcadenti, A., Vermeer, S., Landgren, M., Kroes, H. Y., Yaron, Y., et al. (2009). Comprehensive clinical and molecular assessment of 32 probands with congenital contractural arachnodactyly: report of 14 novel mutations and review of the literature. HUMAN MUTATION, 30(3), 334–341.
Chicago author-date
Callewaert, Bert, Bart Loeys, Anna Ficcadenti, Sascha Vermeer, Magnus Landgren, Hester Y Kroes, Yuval Yaron, et al. 2009. “Comprehensive Clinical and Molecular Assessment of 32 Probands with Congenital Contractural Arachnodactyly: Report of 14 Novel Mutations and Review of the Literature.” Human Mutation 30 (3): 334–341.
Chicago author-date (all authors)
Callewaert, Bert, Bart Loeys, Anna Ficcadenti, Sascha Vermeer, Magnus Landgren, Hester Y Kroes, Yuval Yaron, Michael Pope, Nicola Foulds, Odile Boute, Francisco Galán, Helen Kingston, Nathalie Van der Aa, Iratxe Salcedo, Marielle E Swinkels, Carina Wallgren-Pettersson, Orazio Gabreilli, Julie De Backer, Paul Coucke, and Anne De Paepe. 2009. “Comprehensive Clinical and Molecular Assessment of 32 Probands with Congenital Contractural Arachnodactyly: Report of 14 Novel Mutations and Review of the Literature.” Human Mutation 30 (3): 334–341.
Vancouver
1.
Callewaert B, Loeys B, Ficcadenti A, Vermeer S, Landgren M, Kroes HY, et al. Comprehensive clinical and molecular assessment of 32 probands with congenital contractural arachnodactyly: report of 14 novel mutations and review of the literature. HUMAN MUTATION. 2009;30(3):334–41.
IEEE
[1]
B. Callewaert et al., “Comprehensive clinical and molecular assessment of 32 probands with congenital contractural arachnodactyly: report of 14 novel mutations and review of the literature,” HUMAN MUTATION, vol. 30, no. 3, pp. 334–341, 2009.
@article{627148,
  author       = {Callewaert, Bert and Loeys, Bart and Ficcadenti, Anna and Vermeer, Sascha and Landgren, Magnus and Kroes, Hester Y and Yaron, Yuval and Pope, Michael and Foulds, Nicola and Boute, Odile and Galán, Francisco and Kingston, Helen and Van der Aa, Nathalie and Salcedo, Iratxe and Swinkels, Marielle E and Wallgren-Pettersson, Carina and Gabreilli, Orazio and De Backer, Julie and Coucke, Paul and De Paepe, Anne},
  issn         = {1059-7794},
  journal      = {HUMAN MUTATION},
  keywords     = {MICE,FAMILY,MICROFIBRILS,BEALS-SYNDROME,FIBRILLIN-2,GENE,FBN2 MUTATIONS,congenital contractural arachnodactyly,CCA,FBN2,fibrillin 2,genotype-phenotype,MARFAN-SYNDROME},
  language     = {eng},
  number       = {3},
  pages        = {334--341},
  title        = {Comprehensive clinical and molecular assessment of 32 probands with congenital contractural arachnodactyly: report of 14 novel mutations and review of the literature},
  url          = {http://dx.doi.org/10.1002/humu.20854},
  volume       = {30},
  year         = {2009},
}

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