BBGRE: brain and body genetic resource exchange-Reference-Cited by-同舟云学术

BBGRE: brain and body genetic resource exchange

Published:2013-01-01 Issue: Volume:2013 Page:
ISSN:1758-0463
Container-title:Database
language:en
Short-container-title:

Author:

Ahn Joo Wook¹,Dixit Abhishek¹¹,Johnston Caroline¹¹,Ogilvie Caroline M.¹,Collier David A.¹,Curran Sarah¹,Dobson Richard J. B.¹¹

Affiliation:

1. Department of Cytogenetics, Guy's and St Thomas NHS Foundation Trust, London, SE1 9RT, UK, 2MRC Social, Genetic and Developmental Psychiatry Centre, Institute of Psychiatry, King's College London, De Crespigny Park, London, SE5 8AF and 3NIHR Biomedical Research Centre for Mental Health at South London and Maudsley NHS Foundation, London, SE5 8AF

Publisher

Oxford University Press (OUP)

Subject

General Agricultural and Biological Sciences,General Biochemistry, Genetics and Molecular Biology,Information Systems

Link

http://academic.oup.com/database/article-pdf/doi/10.1093/database/bat067/11197858/bat067.pdf

Reference14 articles.

1. Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies;Miller;Am. J. Hum. Genet.,2010

2. A new chromosome 17q21.31 microdeletion syndrome associated with a common inversion polymorphism;Koolen;Nat. Genet.,2006

3. A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures;Sharp;Nat. Genet.,2008

4. High-resolution mapping and analysis of copy number variations in the human genome: a data resource for clinical and research applications;Shaikh;Genome Res.,2009

5. Detection of large-scale variation in the human genome;Iafrate;Nat. Genet.,2004

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2. Parental Origin of Interstitial Duplications at 15q11.2-q13.3 in Schizophrenia and Neurodevelopmental Disorders;PLOS Genetics;2016-05-06

3. Microdeletions ofELP4Are Associated with Language Impairment, Autism Spectrum Disorder, and Mental Retardation;Human Mutation;2015-06-30