Ghent University Academic Bibliography

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Microhomology-mediated mechanisms underlie non-recurrent disease-causing microdeletions of the FOXL2 gene or its regulatory domain

Hannah Verdin (UGent) , Barbara D'haene (UGent) , DIANE BEYSEN (UGent) , Yana Novikova (UGent) , Björn Menten (UGent) , Tom Sante (UGent) , Pablo Lapunzina, Julian Nevado, Claudio MB Carvalho, James R Lupski, et al.

(2013) PLOS GENETICS. 9(3).
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- Conference Paper
- C3
Mitotic microhomology-mediated replication-based mechanisms underlie non-recurrent pathogenic microdeletions of the FOXL2 gene or its regulatory domain

Hannah Verdin (UGent) , Barbara D'haene (UGent) , DIANE BEYSEN (UGent) , Yana Novikova (UGent) , Björn Menten (UGent) , Tom Sante (UGent) , Pablo Lapunzina, Julian Nevado, Claudia Carvalho, James Lupski, et al.

(2013) Belgian Society of Human Genetics, 13th Annual meeting, Abstracts.
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- Conference Paper
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High-resolution breakpoint mapping of 10 regulatory and 32 FOXL2 encompassing deletions in BPES using targeted microarrays

Hannah Verdin (UGent) , Barbara D'haene (UGent) , Yana Novikova (UGent) , Pablo Lapunzina, Julian Nevado, Björn Menten (UGent) and Elfride De Baere (UGent)

(2011) European Human Genetics conference, Abstracts.
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- Conference Paper
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Mitotic microhomology-mediated replication-based mechanisms underlie non-recurrent pathogenic microdeletions of the FOXL2 gene or its regulatory domain

Hannah Verdin (UGent) , Barbara D'haene (UGent) , Yana Novikova (UGent) , DIANE BEYSEN (UGent) , Pablo Lapunzina, Julian Nevado, Claudia Carvalho, James Lupski, Björn Menten (UGent) and Elfride De Baere (UGent)

(2011) Abstracts of the 12th International congress of Human Genetics (ICHG) ; 61st Annual meeting of the American Society of Human Genetics (ASHG).

Academic Bibliography

Microhomology-mediated mechanisms underlie non-recurrent disease-causing microdeletions of the FOXL2 gene or its regulatory domain

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

High-resolution breakpoint mapping of 10 regulatory and 32 FOXL2 encompassing deletions in BPES using targeted microarrays

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

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