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A familial PLCB4 mutation causing auriculocondylar syndrome..:
Nabil, Amira
;
El Shafei, Sahar
;
El Shakankiri, Nihal M.
...
European Journal of Medical Genetics. 63 (2020) 6 - p. 103917 , 2020
Link:
https://doi.org/10.1016/j.ejmg.2020.103917
RT Journal T1
A familial PLCB4 mutation causing auriculocondylar syndrome 2 with variable severity
UL https://suche.suub.uni-bremen.de/peid=cr-10.1016_j.ejmg.2020.103917&Exemplar=1&LAN=DE A1 Nabil, Amira A1 El Shafei, Sahar A1 El Shakankiri, Nihal M. A1 Habib, Ahmed A1 Morsy, Heba A1 Maddirevula, Sateesh A1 Alkuraya, Fowzan S. PB Elsevier BV YR 2020 SN 1769-7212 JF European Journal of Medical Genetics VO 63 IS 6 SP 103917 LK http://dx.doi.org/https://doi.org/10.1016/j.ejmg.2020.103917 DO https://doi.org/10.1016/j.ejmg.2020.103917 SF ELIB - SuUB Bremen
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