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1 Ergebnisse
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Biallelic variants in Plexin B2 (PLXNB2) cause amelogenesis..:
Smith, Claire E L
;
Laugel-Haushalter, Virginie
;
Hany, Ummey
...
Journal of Medical Genetics. 61 (2024) 7 - p. 689-698 , 2024
Link:
https://doi.org/10.1136/jmg-2023-109728
RT Journal T1
Biallelic variants in Plexin B2 (PLXNB2) cause amelogenesis imperfecta, hearing loss and intellectual disability
UL https://suche.suub.uni-bremen.de/peid=cr-10.1136_jmg-2023-109728&Exemplar=1&LAN=DE A1 Smith, Claire E L A1 Laugel-Haushalter, Virginie A1 Hany, Ummey A1 Best, Sunayna A1 Taylor, Rachel L A1 Poulter, James A A1 Wortmann, Saskia B A1 Feichtinger, Rene G A1 Mayr, Johannes A A1 Al Bahlani, Suhaila A1 Nikolopoulos, Georgios A1 Rigby, Alice A1 Black, Graeme C A1 Watson, Christopher M A1 Mansour, Sahar A1 Inglehearn, Chris F A1 Mighell, Alan J A1 Bloch-Zupan, Agnès PB BMJ YR 2024 SN 0022-2593 SN 1468-6244 JF Journal of Medical Genetics VO 61 IS 7 SP 689 OP 698 LK http://dx.doi.org/https://doi.org/10.1136/jmg-2023-109728 DO https://doi.org/10.1136/jmg-2023-109728 SF ELIB - SuUB Bremen
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