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Mitotic microhomology-mediated replication-based mechanisms underlie non-recurrent pathogenic microdeletions of the FOXL2 gene or its regulatory domain

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Chicago
Verdin, Hannah, Barbara D’haene, DIANE BEYSEN, Yana Novikova, Björn Menten, Tom Sante, Pablo Lapunzina, et al. 2013. “Mitotic Microhomology-mediated Replication-based Mechanisms Underlie Non-recurrent Pathogenic Microdeletions of the FOXL2 Gene or Its Regulatory Domain.” In Belgian Society of Human Genetics, 13th Annual Meeting, Abstracts.
APA
Verdin, H., D’haene, B., BEYSEN, D., Novikova, Y., Menten, B., Sante, T., Lapunzina, P., et al. (2013). Mitotic microhomology-mediated replication-based mechanisms underlie non-recurrent pathogenic microdeletions of the FOXL2 gene or its regulatory domain. Belgian Society of Human Genetics, 13th Annual meeting, Abstracts. Presented at the 13th Annual meeting of the Belgian Society of Human Genetics (BeSHG) : Genetics of human development EXPOsed.
Vancouver
1.
Verdin H, D’haene B, BEYSEN D, Novikova Y, Menten B, Sante T, et al. Mitotic microhomology-mediated replication-based mechanisms underlie non-recurrent pathogenic microdeletions of the FOXL2 gene or its regulatory domain. Belgian Society of Human Genetics, 13th Annual meeting, Abstracts. 2013.
MLA
Verdin, Hannah, Barbara D’haene, DIANE BEYSEN, et al. “Mitotic Microhomology-mediated Replication-based Mechanisms Underlie Non-recurrent Pathogenic Microdeletions of the FOXL2 Gene or Its Regulatory Domain.” Belgian Society of Human Genetics, 13th Annual Meeting, Abstracts. 2013. Print.
@inproceedings{8557606,
  author       = {Verdin, Hannah and D'haene, Barbara and BEYSEN, DIANE and Novikova, Yana and Menten, Bj{\"o}rn and Sante, Tom and Lapunzina, Pablo and Nevado, Julian and Carvalho, Claudia and Lupski, James and De Baere, Elfride},
  booktitle    = {Belgian Society of Human Genetics, 13th Annual meeting, Abstracts},
  language     = {eng},
  location     = {Brussels, Belgium},
  title        = {Mitotic microhomology-mediated replication-based mechanisms underlie non-recurrent pathogenic microdeletions of the FOXL2 gene or its regulatory domain},
  year         = {2013},
}