Whole exome sequencing in females with autism implicates novel and candidate genes.
about
Recent Advances in Autism Spectrum Disorders: Applications of Whole Exome Sequencing TechnologyGenetics of Autism Spectrum Disorder: Current Status and Possible Clinical Applications5p deletions: Current knowledge and future directions.Loss of function of PCDH12 underlies recessive microcephaly mimicking intrauterine infectionComprehensive behavioral phenotyping of a new Semaphorin 3 F mutant mouseWhole exome sequencing reveals inherited and de novo variants in autism spectrum disorder: a trio study from Saudi familiesHigh-resolution chromosome ideogram representation of currently recognized genes for autism spectrum disordersPregnancy at Advanced Maternal Age Affects Behavior and Hippocampal Gene Expression in Mouse Offspring.Altered gene expression in early postnatal monoamine oxidase A knockout mice.Clinical and molecular characterization of a de novo 19p13.3 microdeletionαT-catenin in restricted brain cell types and its potential connection to autism.Preliminary assessment of pre-morbid DNA methylation in individuals at high genetic risk of mood disordersRegulation of neuronal migration, an emerging topic in autism spectrum disorders.NGS Technologies as a Turning Point in Rare Disease Research , Diagnosis and Treatment.Regulation of neural circuit formation by protocadherins.ELAVL2-regulated transcriptional and splicing networks in human neurons link neurodevelopment and autism.Autism genetics - an overview.Exploiting aberrant mRNA expression in autism for gene discovery and diagnosis.Syndrome disintegration: Exome sequencing reveals that Fitzsimmons syndrome is a co-occurrence of multiple events.
P2860
Q26744368-1420E0D4-2B52-4A90-900D-390D718E4899Q26771770-745FDBBE-743E-4F4B-944D-B3DFD63DFD9FQ26800129-0EA563B8-DE5C-41B0-A654-B202563044F7Q30355867-9B013E93-7912-4B89-984D-732DE0EC630AQ30391378-3DD0219F-5920-4561-B0CB-8B1F33F8C296Q33916084-4DA26D88-8B14-43F7-AB17-0B4B80AACC58Q35381777-AEA3EEFA-E243-4F7C-ABCC-15EF2967F58BQ36318604-4E24271F-D99B-4DF1-A781-A009028F29BFQ36378850-13CA50B2-2DF3-4E23-94DD-5591B0936F3FQ36942065-6FED34ED-A554-4A26-B0D8-2A82165738CCQ37024399-FAD2F849-C3D4-4868-BC82-0FD1FDB0BE9AQ37221976-E3330501-B38F-46D1-9CDA-4A91BFA4D820Q38612196-0665A1F5-F5DE-4656-8B28-17E9D99DAC12Q38655437-CA68CCC1-29D8-4142-A14B-90940E4C2367Q38718127-7327191E-0031-4936-823A-4D208E441427Q38766679-40F34213-ED21-40FA-AEDE-116BA9C5AFCCQ38981431-D0C9C14F-17F2-4C55-AE0F-52E83262C0F2Q39807149-C7539A95-586D-4555-B86B-2409D2956CDEQ53110067-62207E7D-CF0A-4A79-8A68-FA3437F6E6C2
P2860
Whole exome sequencing in females with autism implicates novel and candidate genes.
description
2015 nî lūn-bûn
@nan
2015 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2015 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2015年の論文
@ja
2015年学术文章
@wuu
2015年学术文章
@zh-cn
2015年学术文章
@zh-hans
2015年学术文章
@zh-my
2015年学术文章
@zh-sg
2015年學術文章
@yue
name
Whole exome sequencing in females with autism implicates novel and candidate genes.
@ast
Whole exome sequencing in females with autism implicates novel and candidate genes.
@en
type
label
Whole exome sequencing in females with autism implicates novel and candidate genes.
@ast
Whole exome sequencing in females with autism implicates novel and candidate genes.
@en
prefLabel
Whole exome sequencing in females with autism implicates novel and candidate genes.
@ast
Whole exome sequencing in females with autism implicates novel and candidate genes.
@en
P2093
P2860
P356
P1476
Whole exome sequencing in females with autism implicates novel and candidate genes.
@en
P2093
Dietrich A Stephan
Merlin G Butler
Syed K Rafi
Waheeda Hossain
P2860
P304
P356
10.3390/IJMS16011312
P407
P577
2015-01-07T00:00:00Z