Detalles de la búsqueda
1.
Synaptic, transcriptional and chromatin genes disrupted in autism.
Nature
; 515(7526): 209-15, 2014 Nov 13.
Artículo
en Inglés
| MEDLINE | ID: mdl-25363760
2.
Whole-Genome Sequencing and Integrative Genomic Analysis Approach on Two 22q11.2 Deletion Syndrome Family Trios for Genotype to Phenotype Correlations.
Hum Mutat
; 36(8): 797-807, 2015 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-25981510
3.
The disruption of Celf6, a gene identified by translational profiling of serotonergic neurons, results in autism-related behaviors.
J Neurosci
; 33(7): 2732-53, 2013 Feb 13.
Artículo
en Inglés
| MEDLINE | ID: mdl-23407934
4.
Spectrum of elastin sequence variants and cardiovascular phenotypes in 49 patients with Williams-Beuren syndrome.
Am J Med Genet A
; 161A(3): 527-33, 2013 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-23401415
5.
The effect of graphitized carbon on the adsorption and photocatalytic degradation of methylene blue over TiO2/C composites.
RSC Adv
; 10(67): 40830-40842, 2020 Nov 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-35519181
6.
Whole-Genome Sequencing and iPLEX MassARRAY Genotyping Map an EMS-Induced Mutation Affecting Cell Competition in Drosophila melanogaster.
G3 (Bethesda)
; 6(10): 3207-3217, 2016 10 13.
Artículo
en Inglés
| MEDLINE | ID: mdl-27574103
7.
Reciprocal Relationship between Head Size, an Autism Endophenotype, and Gene Dosage at 19p13.12 Points to AKAP8 and AKAP8L.
PLoS One
; 10(6): e0129270, 2015.
Artículo
en Inglés
| MEDLINE | ID: mdl-26076356
8.
A Novel C-Terminal CIB2 (Calcium and Integrin Binding Protein 2) Mutation Associated with Non-Syndromic Hearing Loss in a Hispanic Family.
PLoS One
; 10(10): e0133082, 2015.
Artículo
en Inglés
| MEDLINE | ID: mdl-26426422
9.
Coex-Rank: An approach incorporating co-expression information for combined analysis of microarray data.
J Integr Bioinform
; 9(1): 208, 2012 Jul 30.
Artículo
en Inglés
| MEDLINE | ID: mdl-22842118
10.
Correction: A Novel C-Terminal CIB2 (Calcium and Integrin Binding Protein 2) Mutation Associated with Non-Syndromic Hearing Loss in a Hispanic Family.
PLoS One
; 10(10): e0141259, 2015.
Artículo
en Inglés
| MEDLINE | ID: mdl-26473954
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