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Author/Creator Reyniers, Edwin

1. Genetic variants in the KDM6B gene are associated with neurodevelopmental delays and dysmorphic features. Issue 7 (23rd May 2019)

Authors:
Stolerman, Elliot S.; Francisco, Elizabeth; Stallworth, Jennifer L.; Jones, Julie R.; Monaghan, Kristin G.; Keller‐Ramey, Jennifer; Person, Richard; Wentzensen, Ingrid M.; McWalter, Kirsty; Keren, Boris; Heron, Benedicte; Nava, Caroline; Heron, Delphine; Kim, Katherine; Burton, Barbara; Al‐Musafr...
Journal:
American journal of medical genetics
Issue:
Volume 179:Issue 7(2019)
Page Start:
1276
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

2. Further molecular and clinical delineation of co-locating 17p13.3 microdeletions and microduplications that show distinctive phenotypes. Issue 5 (7th May 2010)

Authors:
Bruno, Damien L; Anderlid, Britt-Marie; Lindstrand, Anna; van Ravenswaaij-Arts, Conny; Ganesamoorthy, Devika; Lundin, Johanna; Martin, Christa Lese; Douglas, Jessica; Nowak, Catherine; Adam, Margaret P; Kooy, R Frank; Van der Aa, Nathalie; Reyniers, Edwin; Vandeweyer, Geert; Stolte-Dijkstra, Iren...
Journal:
Journal of medical genetics
Issue:
Volume 47:Issue 5(2010)
Page Start:
299
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗