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
3.
Advances in the Production and Batch Reformatting of Phage Antibody Libraries.
Mol Biotechnol
; 61(11): 801-815, 2019 Nov.
Article
in English
| MEDLINE | ID: mdl-31468301
4.
Next-generation DNA sequencing identifies novel gene variants and pathways involved in specific language impairment.
Sci Rep
; 7: 46105, 2017 04 25.
Article
in English
| MEDLINE | ID: mdl-28440294
5.
Genome-wide analysis identifies a role for common copy number variants in specific language impairment.
Eur J Hum Genet
; 23(10): 1370-7, 2015 Oct.
Article
in English
| MEDLINE | ID: mdl-25585696
6.
Genome-Wide Studies of Specific Language Impairment.
Curr Behav Neurosci Rep
; 1(4): 242-250, 2014.
Article
in English
| MEDLINE | ID: mdl-25411653
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