Supplemental Appendix

Sandrine Caburet , Abdelkader Heddar , Elodie Dardillac , Helene Creux
Annals of Vascular Surgery 37 262 -331

2016
CO24 - Étude du génome de familles avec insuffisances ovariennes prématurées

S. Christin-Maitre , P. Bouchard , N. Bourcigaux , D. Bacq
Annales D Endocrinologie 67 ( 5) 391

2006
Allelic reduction of Dlx5 and Dlx6 results in early follicular depletion: a new mouse model of primary ovarian insufficiency

K. Bouhali , A. Dipietromaria , A. Fontaine , S. Caburet
Human Molecular Genetics 20 ( 13) 2642 -2650

20
2011
Mechanisms of Mendelian dominance.

R.A. Veitia , S. Caburet , J.A. Birchler
Clinical Genetics 93 ( 3) 419 -428

26
2018
A non‐sense MCM9 mutation in a familial case of primary ovarian insufficiency

F. Fauchereau , S. Shalev , E. Chervinsky , R. Beck-Fruchter
Clinical Genetics 89 ( 5) 603 -607

40
2016
The genetic make-up of ovarian development and function: the focus on the transcription factor FOXL2

M. Elzaiat , A.-L. Todeschini , S. Caburet , R.A. Veitia
Clinical Genetics 91 ( 2) 173 -182

41
2017
A recurrent polyalanine expansion in the transcription factor FOXL2 induces extensive nuclear and cytoplasmic protein aggregation

S Caburet , A Demarez , L Moumne , M Fellous
Journal of Medical Genetics 41 ( 12) 932 -936

86
2004
Whole genome analysis of DNA replication and genetic alterations

J Herrick , C Chiara , S Caburet , A Bensimon
CYTOGENETICS AND CELL GENETICS 85 ( 1-2) 19 -19

1999
LADON, a natural antisense transcript of NODAL, promotes metastasis in melanoma by repressing NDRG1

Dutriaux Annie , Diazzi Serena , Caburet Sandrine , Bresesti Chiara
bioRxiv

2020