Van Reyk, Olivia
14  Ergebnisse:
Personensuche X
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1

Beyond 'speech delay': Expanding the phenotype of BRPF1-rel..:

Morison, Lottie D. ; Van Reyk, Olivia ; Baker, Emma...
European Journal of Medical Genetics.  68 (2024)  - p. 104923 , 2024
 
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3

CDK13-related disorder: a deep characterization of speech a..:

Morison, Lottie D. ; van Reyk, Olivia ; Forbes, Elana...
European Journal of Human Genetics.  31 (2023)  7 - p. 793-804 , 2023
 
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6

Expanding the speech and language phenotype in Koolen-de Vr..:

St John, Miya ; van Reyk, Olivia ; Koolen, David A....
European Journal of Human Genetics.  31 (2022)  5 - p. 531-540 , 2022
 
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7

Self‐reported impact of developmental stuttering across the..:

Boyce, Jessica O. ; Jackson, Victoria E. ; van Reyk, Olivia...
Developmental Medicine & Child Neurology.  64 (2022)  10 - p. 1297-1306 , 2022
 
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14

Severe childhood speech disorder:Gene discovery highlights ..:

Hildebrand, Michael S ; Jackson, Victoria E ; Scerri, Thomas S...
Hildebrand , M S , Jackson , V E , Scerri , T S , Van Reyk , O , Coleman , M , Braden , R O , Turner , S , Rigbye , K A , Boys , A , Barton , S , Webster , R , Fahey , M , Saunders , K , Parry-Fielder , B , Paxton , G , Hayman , M , Coman , D , Goel , H , Baxter , A , Ma , A , Davis , N , Reilly , S , Delatycki , M , Liégeois , F J , Connelly , A , Gecz , J , Fisher , S E , Amor , D J , Scheffer , I E , Bahlo , M & Morgan , A T 2020 , ' Severe childhood speech disorder : Gene discovery highlights transcriptional dysregulation ' , Neurology , vol. 94 , no. 20 , pp. e2148-e2167 . https://doi.org/10.1212/WNL.0000000000009441.  , 2020
 
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