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1.
De novo and rare inherited copy-number variations in the hemiplegic form of cerebral palsy.
Genet Med
; 20(2): 172-180, 2018 02.
Article
in English
| MEDLINE | ID: mdl-28771244
2.
Functional impact of global rare copy number variation in autism spectrum disorders.
Nature
; 466(7304): 368-72, 2010 Jul 15.
Article
in English
| MEDLINE | ID: mdl-20531469
3.
A genome-wide scan for common alleles affecting risk for autism.
Hum Mol Genet
; 19(20): 4072-82, 2010 Oct 15.
Article
in English
| MEDLINE | ID: mdl-20663923
4.
The Centre for Modeling Human Disease Gene Trap resource.
Nucleic Acids Res
; 32(Database issue): D557-9, 2004 Jan 01.
Article
in English
| MEDLINE | ID: mdl-14681480
5.
Transcriptome-wide characterization of the endogenous miR-34A-p53 tumor suppressor network.
Oncotarget
; 7(31): 49611-49622, 2016 Aug 02.
Article
in English
| MEDLINE | ID: mdl-27391063
6.
Gene and miRNA expression profiles in autism spectrum disorders.
Brain Res
; 1380: 85-97, 2011 Mar 22.
Article
in English
| MEDLINE | ID: mdl-20868653
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