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Evaluation and application of denaturing HPLC for mutation detection in Marfan syndrome: Identification of 20 novel mutations and two novel polymorphisms in the FBN1 gene.

(2002) HUMAN MUTATION. 19(4). p.443-456
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Chicago
MATYAS, G, Anne De Paepe, D HALLIDAY, C BOILEAU, G PALS, and B STEINMANN. 2002. “Evaluation and Application of Denaturing HPLC for Mutation Detection in Marfan Syndrome: Identification of 20 Novel Mutations and Two Novel Polymorphisms in the FBN1 Gene.” Human Mutation 19 (4): 443–456.
APA
MATYAS, G., De Paepe, A., HALLIDAY, D., BOILEAU, C., PALS, G., & STEINMANN, B. (2002). Evaluation and application of denaturing HPLC for mutation detection in Marfan syndrome: Identification of 20 novel mutations and two novel polymorphisms in the FBN1 gene. HUMAN MUTATION, 19(4), 443–456.
Vancouver
1.
MATYAS G, De Paepe A, HALLIDAY D, BOILEAU C, PALS G, STEINMANN B. Evaluation and application of denaturing HPLC for mutation detection in Marfan syndrome: Identification of 20 novel mutations and two novel polymorphisms in the FBN1 gene. HUMAN MUTATION. 2002;19(4):443–56.
MLA
MATYAS, G, Anne De Paepe, D HALLIDAY, et al. “Evaluation and Application of Denaturing HPLC for Mutation Detection in Marfan Syndrome: Identification of 20 Novel Mutations and Two Novel Polymorphisms in the FBN1 Gene.” HUMAN MUTATION 19.4 (2002): 443–456. Print.
@article{149703,
  author       = {MATYAS, G and De Paepe, Anne and HALLIDAY, D and BOILEAU, C and PALS, G and STEINMANN, B},
  issn         = {1059-7794},
  journal      = {HUMAN MUTATION},
  language     = {eng},
  number       = {4},
  pages        = {443--456},
  title        = {Evaluation and application of denaturing HPLC for mutation detection in Marfan syndrome: Identification of 20 novel mutations and two novel polymorphisms in the FBN1 gene.},
  volume       = {19},
  year         = {2002},
}

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