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A homozygous FANCM mutation underlies a familial case of no..:
Fouquet, Baptiste
;
Pawlikowska, Patrycja
;
Caburet, Sandrine
...
eLife. 6 (2017) - p. , 2017
Link:
https://doi.org/10.7554/elife.30490
RT Journal T1
A homozygous FANCM mutation underlies a familial case of non-syndromic primary ovarian insufficiency
UL https://suche.suub.uni-bremen.de/peid=cr-10.7554_elife.30490&Exemplar=1&LAN=DE A1 Fouquet, Baptiste A1 Pawlikowska, Patrycja A1 Caburet, Sandrine A1 Guigon, Celine A1 Mäkinen, Marika A1 Tanner, Laura A1 Hietala, Marja A1 Urbanska, Kaja A1 Bellutti, Laura A1 Legois, Bérangère A1 Bessieres, Bettina A1 Gougeon, Alain A1 Benachi, Alexandra A1 Livera, Gabriel A1 Rosselli, Filippo A1 Veitia, Reiner A A1 Misrahi, Micheline PB eLife Sciences Publications, Ltd YR 2017 SN 2050-084X JF eLife VO 6 LK http://dx.doi.org/https://doi.org/10.7554/elife.30490 DO https://doi.org/10.7554/elife.30490 SF ELIB - SuUB Bremen
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