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8q21.11 microdeletion syndrome: Delineation of HEY1 as a ca..:
Ben Ayed, Ikhlas
;
Bouzid, Amal
;
Kammoun, Fatma
...
Molecular Genetics & Genomic Medicine. 9 (2021) 11 - p. , 2021
Link:
https://doi.org/10.1002/mgg3.1811
RT Journal T1
8q21.11 microdeletion syndrome: Delineation of HEY1 as a candidate gene in neurodevelopmental and cardiac defects
UL https://suche.suub.uni-bremen.de/peid=cr-10.1002_mgg3.1811&Exemplar=1&LAN=DE A1 Ben Ayed, Ikhlas A1 Bouzid, Amal A1 Kammoun, Fatma A1 souissi, Amal A1 Jallouli, Olfa A1 Mallouli, Salma A1 Guidara, Souhir A1 Loukil, Salma A1 Aloulou, Hajer A1 Jbeli, Fida A1 Aouichaoui, Sahar A1 Abid, Dorra A1 Abdelhedi, Fatma A1 Triki, Chahnez A1 Kamoun, Hassen A1 Masmoudi, Saber PB Wiley YR 2021 SN 2324-9269 SN 2324-9269 JF Molecular Genetics & Genomic Medicine VO 9 IS 11 LK http://dx.doi.org/https://doi.org/10.1002/mgg3.1811 DO https://doi.org/10.1002/mgg3.1811 SF ELIB - SuUB Bremen
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