Frequency and Complexity of De Novo Structural Mutation in Autism.
about
Defining Disease, Diagnosis, and Translational Medicine within a Homeostatic Perturbation Paradigm: The National Institutes of Health Undiagnosed Diseases Program Experience.The psoriasis-associated deletion of late cornified envelope genes LCE3B and LCE3C has been maintained under balancing selection since Human Denisovan divergence.Association Between Mitochondrial DNA Haplogroup Variation and Autism Spectrum Disorders.TIDDIT, an efficient and comprehensive structural variant caller for massive parallel sequencing data.Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects.Opportunities for an enhanced integration of neuroscience and genomics.Whole genome sequencing in psychiatric disorders: the WGSPD consortium.A Comprehensive Workflow for Read Depth-Based Identification of Copy-Number Variation from Whole-Genome Sequence Data.SV2: Accurate Structural Variation Genotyping and De Novo Mutation Detection from Whole Genomes.Mitochondrial Etiology of Neuropsychiatric Disorders.Settling the score: variant prioritization and Mendelian disease.Robust identification of deletions in exome and genome sequence data based on clustering of Mendelian errors.Two de novo novel mutations in one SHANK3 allele in a patient with autism and moderate intellectual disability.The Balance of Th17 versus Treg Cells in Autoimmunity.Mutations (DNMs) in Autism Spectrum Disorder (ASD): Pathway and Network Analysis
P2860
Q33729428-6C46C0B1-5778-4666-9AD2-99B030A8DED2Q36213630-DA48A037-B918-4013-8BD1-6A9C61238E2EQ38612433-E7960F09-FF0D-4D8B-88CA-B76C19330442Q38637936-E66E3F55-C7F1-41BD-A0F4-850407FC8CACQ39217627-4E46B15A-6784-4BD3-B43D-9938BA677263Q45070857-8B9DBD62-32A6-40CF-BB91-A4E9ADC51CF8Q45950157-4C218294-C0EF-4FBA-8EC7-A8EDC3AC18C0Q47205107-0C2E1552-E86B-4366-82C1-AF724229696CQ47209971-4E1DBC18-04C6-4ADA-A8A2-F3935D8910ADQ47888701-36442B75-9F69-4C2C-987D-27F5598D1091Q52544730-D6E98C53-EC8A-4E95-BB02-0D3B087E2D7AQ52661383-F85DE277-B14F-454C-9B9C-864CDD2423E5Q52697198-E5273911-1491-4788-A9A1-934C9E460FB2Q55314022-BC4A9A46-38A1-4962-A20D-9DB39D5871ABQ57300010-ED882D24-B162-456C-8107-C6F3386CC635
P2860
Frequency and Complexity of De Novo Structural Mutation in Autism.
description
2016 nî lūn-bûn
@nan
2016 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2016 թվականի մարտին հրատարակված գիտական հոդված
@hy
2016年の論文
@ja
2016年論文
@yue
2016年論文
@zh-hant
2016年論文
@zh-hk
2016年論文
@zh-mo
2016年論文
@zh-tw
2016年论文
@wuu
name
Frequency and Complexity of De Novo Structural Mutation in Autism.
@ast
Frequency and Complexity of De Novo Structural Mutation in Autism.
@en
Frequency and Complexity of De Novo Structural Mutation in Autism.
@nl
type
label
Frequency and Complexity of De Novo Structural Mutation in Autism.
@ast
Frequency and Complexity of De Novo Structural Mutation in Autism.
@en
Frequency and Complexity of De Novo Structural Mutation in Autism.
@nl
prefLabel
Frequency and Complexity of De Novo Structural Mutation in Autism.
@ast
Frequency and Complexity of De Novo Structural Mutation in Autism.
@en
Frequency and Complexity of De Novo Structural Mutation in Autism.
@nl
P2093
P2860
P50
P1476
Frequency and Complexity of De Novo Structural Mutation in Autism.
@en
P2093
Abhishek Bhandari
Alexandra G Moyzis
Alysson R Muotri
Amanda C Watts
Amina Noor
Charles M Strom
Christina Corsello
Daniel J Barrera
Danny Antaki
Dheeraj Malhotra
P2860
P304
P356
10.1016/J.AJHG.2016.02.018
P407
P577
2016-03-23T00:00:00Z