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Overlap of polymicrogyria, hydrocephalus, and Joubert syndrome in a family with novel truncating mutations in ADGRG1/GPR56 and KIAA0556

Cauley, Edmund S; Hamed, Ahlam; Mohamed, Inaam N.; Elseed, Maha; Martinez, Samantha; Yahia, Ashraf; Abozar, Fatima; Abubakr, Rayan; Koko, Mahmoud; Elsayed, Liena; Piao, Xianhua; Salih, Mustafa A.; Manzini, M Chiara (Neurogenetics, 2019)

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- Hydrocephalus (1)
- Joubert syndrome (1)
- Lissencephaly (1)
- Polymicrogyria. (1)
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- 2019 (1)
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