Original language | English |
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Pages (from-to) | 42-43 |
Journal | Hormone Research in Paediatrics |
Volume | 94 |
Issue number | SUPPL 1 |
Publication status | Published - Sept 2021 |
Individuals with NR5A1 (SF1) mutations and atypical sex development and their asymptomatic family member carriers are at high risk of hyposplenism
Celien Grijp, Simon Tavernier, Jana Neirinck, Maha Abdulhadi-Atwan, Julie Van De Velde, Dorien Baetens, Hannah Verdin, Lieve Morbee, Elfride De Baere, David Zangen, Carolien Bonroy, Yolande Van Bever, Hennie Bruggenwirth, Clementien Vermont, Sabine Hannema, Yolanda De Rijke, Petra Schelstraete, Filomeen Haerynck, Martine Cools
Research output: Contribution to journal › Meeting Abstract › Academic