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Role of CGH array in the diagnosis of autosomal recessive disease : a case of Ellis-van Creveld syndrome

(2015) PRENATAL DIAGNOSIS. 35(1). p.97-99
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EVC2, PRENATAL-DIAGNOSIS, MUTATIONS

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Citation

Please use this url to cite or link to this publication:

Chicago
D’Ambrosio, Valentina, Carmela Votino, Teresa Cos, Sebastien Boulanger, Annelies Dheedene, Jacques Jani, and Kathelijn Keymolen. 2015. “Role of CGH Array in the Diagnosis of Autosomal Recessive Disease : a Case of Ellis-van Creveld Syndrome.” Prenatal Diagnosis 35 (1): 97–99.
APA
D’Ambrosio, Valentina, Votino, C., Cos, T., Boulanger, S., Dheedene, A., Jani, J., & Keymolen, K. (2015). Role of CGH array in the diagnosis of autosomal recessive disease : a case of Ellis-van Creveld syndrome. PRENATAL DIAGNOSIS, 35(1), 97–99.
Vancouver
1.
D’Ambrosio V, Votino C, Cos T, Boulanger S, Dheedene A, Jani J, et al. Role of CGH array in the diagnosis of autosomal recessive disease : a case of Ellis-van Creveld syndrome. PRENATAL DIAGNOSIS. 2015;35(1):97–9.
MLA
D’Ambrosio, Valentina et al. “Role of CGH Array in the Diagnosis of Autosomal Recessive Disease : a Case of Ellis-van Creveld Syndrome.” PRENATAL DIAGNOSIS 35.1 (2015): 97–99. Print.
@article{5955490,
  author       = {D'Ambrosio, Valentina and Votino, Carmela and Cos, Teresa and Boulanger, Sebastien and Dheedene, Annelies and Jani, Jacques and Keymolen, Kathelijn},
  issn         = {0197-3851},
  journal      = {PRENATAL DIAGNOSIS},
  keywords     = {EVC2,PRENATAL-DIAGNOSIS,MUTATIONS},
  language     = {eng},
  number       = {1},
  pages        = {97--99},
  title        = {Role of CGH array in the diagnosis of autosomal recessive disease : a case of Ellis-van Creveld syndrome},
  url          = {http://dx.doi.org/10.1002/pd.4490},
  volume       = {35},
  year         = {2015},
}

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