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

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

Original language	English
Pages (from-to)	42-43
Journal	Hormone Research in Paediatrics
Volume	94
Issue number	SUPPL 1
Publication status	Published - Sept 2021

Cite this

Grijp, C., Tavernier, S., Neirinck, J., Abdulhadi-Atwan, M., Van De Velde, J., Baetens, D., Verdin, H., Morbee, L., De Baere, E., Zangen, D., Bonroy, C., Van Bever, Y., Bruggenwirth, H., Vermont, C., Hannema, S., De Rijke, Y., Schelstraete, P., Haerynck, F., & Cools, M. (2021). Individuals with NR5A1 (SF1) mutations and atypical sex development and their asymptomatic family member carriers are at high risk of hyposplenism. Hormone Research in Paediatrics, 94(SUPPL 1), 42-43.

@article{0d1270b693d34f96a8b5293479f59487,

title = "Individuals with NR5A1 (SF1) mutations and atypical sex development and their asymptomatic family member carriers are at high risk of hyposplenism",

author = "Celien Grijp and Simon Tavernier and Jana Neirinck and Maha Abdulhadi-Atwan and {Van De Velde}, Julie and Dorien Baetens and Hannah Verdin and Lieve Morbee and {De Baere}, Elfride and David Zangen and Carolien Bonroy and {Van Bever}, Yolande and Hennie Bruggenwirth and Clementien Vermont and Sabine Hannema and {De Rijke}, Yolanda and Petra Schelstraete and Filomeen Haerynck and Martine Cools",

year = "2021",

month = sep,

language = "English",

volume = "94",

pages = "42--43",

journal = "Hormone Research in Paediatrics",

issn = "1663-2818",

publisher = "S. Karger AG",

number = "SUPPL 1",

}

Grijp, C, Tavernier, S, Neirinck, J, Abdulhadi-Atwan, M, Van De Velde, J, Baetens, D, Verdin, H, Morbee, L, De Baere, E, Zangen, D, Bonroy, C, Van Bever, Y, Bruggenwirth, H, Vermont, C, Hannema, S, De Rijke, Y, Schelstraete, P, Haerynck, F & Cools, M 2021, 'Individuals with NR5A1 (SF1) mutations and atypical sex development and their asymptomatic family member carriers are at high risk of hyposplenism', Hormone Research in Paediatrics, vol. 94, no. SUPPL 1, pp. 42-43.

TY - JOUR

T1 - Individuals with NR5A1 (SF1) mutations and atypical sex development and their asymptomatic family member carriers are at high risk of hyposplenism

AU - Grijp, Celien

AU - Tavernier, Simon

AU - Neirinck, Jana

AU - Abdulhadi-Atwan, Maha

AU - Van De Velde, Julie

AU - Baetens, Dorien

AU - Verdin, Hannah

AU - Morbee, Lieve

AU - De Baere, Elfride

AU - Zangen, David

AU - Bonroy, Carolien

AU - Van Bever, Yolande

AU - Bruggenwirth, Hennie

AU - Vermont, Clementien

AU - Hannema, Sabine

AU - De Rijke, Yolanda

AU - Schelstraete, Petra

AU - Haerynck, Filomeen

AU - Cools, Martine

PY - 2021/9

Y1 - 2021/9

M3 - Meeting Abstract

SN - 1663-2818

VL - 94

SP - 42

EP - 43

JO - Hormone Research in Paediatrics

JF - Hormone Research in Paediatrics

IS - SUPPL 1

ER -