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Author/Creator Fee, Timothy

2. Mosaicism of common pathogenic MECP2 variants identified in two males with a clinical diagnosis of Rett syndrome. Issue 10 (4th August 2022)

Authors:
Cooley Coleman, Jessica A.; Fee, Timothy; Bend, Renee; Louie, Raymond; Annese, Fran; Stallworth, Jennifer; Worthington, Jessica; Buchanan, Caroline Black; Everman, David B.; Skinner, Steven; Friez, Michael J.; Jones, Julie R.; Spellicy, Catherine J.
Journal:
American journal of medical genetics
Issue:
Volume 188:Issue 10(2022)
Page Start:
2988
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

3. Functional correlation of genome‐wide DNA methylation profiles in genetic neurodevelopmental disorders. Issue 11 (21st August 2022)

Authors:
Levy, Michael A.; Relator, Raissa; McConkey, Haley; Pranckeviciene, Erinija; Kerkhof, Jennifer; Barat‐Houari, Mouna; Bargiacchi, Sara; Biamino, Elisa; Palomares Bralo, María; Cappuccio, Gerarda; Ciolfi, Andrea; Clarke, Angus; DuPont, Barbara R.; Elting, Mariet W.; Faivre, Laurence; Fee, Timothy; ...
Other Names:
Scott Stuart A. guestEditor.; Wang Kai guestEditor.; Spinner Nancy B. guestEditor.
Journal:
Human mutation
Issue:
Volume 43:Issue 11(2022)
Page Start:
1609
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗