Next generation sequencing coupled to functional genomics implicates FOXP 
pathways in autism and language impairment

Derizioti, Pelagia; O'Roak, B.; Vives, L.; Shendure, J.; Eichler, E.; Fisher, Simon E.

Item

ITEM ACTIONSEXPORT

Add to Basket

Local TagsRelease HistoryDetailsSummary

Released

Talk

Next generation sequencing coupled to functional genomics implicates FOXP pathways in autism and language impairment

MPS-Authors

/persons/resource/persons32809

Derizioti, Pelagia
Language and Genetics Department, MPI for Psycholinguistics, Max Planck Society;

/persons/resource/persons4427

Fisher, Simon E.
Language and Genetics Department, MPI for Psycholinguistics, Max Planck Society;

External Resource

No external resources are shared

Fulltext (restricted access)

There are currently no full texts shared for your IP range.

Fulltext (public)

There are no public fulltexts stored in PuRe

Supplementary Material (public)

There is no public supplementary material available

Citation

Derizioti, P., O'Roak, B., Vives, L., Shendure, J., Eichler, E., & Fisher, S. E. (2012). Next generation sequencing coupled to functional genomics implicates FOXP pathways in autism and language impairment. Talk presented at Capita Selecta in Complex Disease Analysis 2012. Liege, Belgium. 2012-05-30 - 2012-06-01.

Cite as: https://hdl.handle.net/11858/00-001M-0000-000E-7EC1-0

Abstract

There is no abstract available