Microhomology-mediated mechanisms underlie non-recurrent disease-causing microdeletions of the FOXL2 gene or its regulatory domain (Q34629238)

3 August 2017

title

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

1 reference

3 August 2017

James R Lupski

1 reference

3 August 2017

Björn Menten

1 reference

3 August 2017

Hannah Verdin

1 reference

3 August 2017

Barbara D'haene

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3 August 2017

Diane Beysen

1 reference

3 August 2017

Yana Novikova

1 reference

3 August 2017

Tom Sante

1 reference

3 August 2017

Pablo Lapunzina

1 reference

3 August 2017

Julian Nevado

1 reference

3 August 2017

Claudia M B Carvalho

1 reference

3 August 2017

Elfride De Baere

1 reference

3 August 2017

publication date

14 March 2013

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3 August 2017

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3 August 2017

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3 August 2017

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3 August 2017

page(s)

e1003358

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Creative Commons Attribution 4.0 International

3 August 2017

start time

14 March 2013

1 reference

April 2022 Public Data File from Crossref

copyrighted

0 references

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7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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Spectrum of FOXL2 gene mutations in blepharophimosis-ptosis-epicanthus inversus (BPES) families demonstrates a genotype--phenotype correlation

7 July 2018

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7 July 2018

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Identifiers

DOI

10.1371/JOURNAL.PGEN.1003358

1 reference

3 August 2017

1 reference

3 August 2017

1 reference