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A de novo 10p11.23‐p12.1 deletion recapitulates the phenoty..:
Abdelhedi, Fatma
;
El Khattabi, Laila
;
Essid, Nouha
...
American Journal of Medical Genetics Part A. 170 (2016) 7 - p. 1912-1917 , 2016
Link:
https://doi.org/10.1002/ajmg.a.37686
RT Journal T1 <Title>A de novo 10p11.23‐p12.1 deletion recapitulates the phenotype observed in WAC mutations and strengthens the role of WAC in intellectual disability and behavior disorders</Title> UL https://suche.suub.uni-bremen.de/peid=cr-10.1002_ajmg.a.37686&Exemplar=1&LAN=DE A1 Abdelhedi, Fatma A1 El Khattabi, Laila A1 Essid, Nouha A1 Viot, Geraldine A1 Letessier, Dominique A1 Lebbar, Aziza A1 Dupont, Jean‐Michel PB Wiley YR 2016 SN 1552-4825 SN 1552-4833 JF American Journal of Medical Genetics Part A VO 170 IS 7 SP 1912 OP 1917 LK http://dx.doi.org/https://doi.org/10.1002/ajmg.a.37686 DO https://doi.org/10.1002/ajmg.a.37686 SF ELIB - SuUB Bremen
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