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High-resolution breakpoint mapping of 38 regulatory and FOXL2 encompassing deletions in BPES using targeted microarrays

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Chicago
Verdin, Hannah, Barbara D’haene, Yana Novikova, Pablo Lapunzina, Julian Nevado, Björn Menten, and Elfride De Baere. 2011. “High-resolution Breakpoint Mapping of 38 Regulatory and FOXL2 Encompassing Deletions in BPES Using Targeted Microarrays.” In Genomic Disorders, Abstracts.
APA
Verdin, H., D’haene, B., Novikova, Y., Lapunzina, P., Nevado, J., Menten, B., & De Baere, E. (2011). High-resolution breakpoint mapping of 38 regulatory and FOXL2 encompassing deletions in BPES using targeted microarrays. Genomic Disorders, Abstracts. Presented at the Genomic Disorders 2011: The genomics of rare diseases.
Vancouver
1.
Verdin H, D’haene B, Novikova Y, Lapunzina P, Nevado J, Menten B, et al. High-resolution breakpoint mapping of 38 regulatory and FOXL2 encompassing deletions in BPES using targeted microarrays. Genomic Disorders, Abstracts. 2011.
MLA
Verdin, Hannah, Barbara D’haene, Yana Novikova, et al. “High-resolution Breakpoint Mapping of 38 Regulatory and FOXL2 Encompassing Deletions in BPES Using Targeted Microarrays.” Genomic Disorders, Abstracts. 2011. Print.
@inproceedings{8552201,
  author       = {Verdin, Hannah and D'haene, Barbara and Novikova, Yana and Lapunzina, Pablo and Nevado, Julian and Menten, Bj{\"o}rn and De Baere, Elfride},
  booktitle    = {Genomic Disorders, Abstracts},
  language     = {eng},
  location     = {Hinxton, UK},
  title        = {High-resolution breakpoint mapping of 38 regulatory and FOXL2 encompassing deletions in BPES using targeted microarrays},
  year         = {2011},
}