Search details
1.
Exome sequencing in an admixed isolated population indicates NFXL1 variants confer a risk for specific language impairment.
PLoS Genet
; 11(3): e1004925, 2015 Mar.
Article
in English
| MEDLINE | ID: mdl-25781923
2.
Correction: Exome Sequencing in an Admixed Isolated Population Indicates NFXL1 Variants Confer a Risk for Specific Language Impairment.
PLoS Genet
; 11(6): e1005336, 2015 Jun.
Article
in English
| MEDLINE | ID: mdl-26114769
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