(Q57419525)

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Phenotypic variations on the theme of CNVs

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title

Phenotypic variations on the theme of CNVs (English)

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George Kirov

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Michael C O'Donovan

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Michael C O'Donovan

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1

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author name string

Michael J Owen

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3

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language of work or name

English

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publication date

December 2008

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published in

Nature Genetics

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volume

40

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page(s)

1392-1393

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issue

12

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exact match

https://scigraph.springernature.com/pub.10.1038/ng1208-1392

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Large-scale copy number polymorphism in the human genome

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Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG1208-1392

retrieved

21 January 2018

Global variation in copy number in the human genome

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Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG1208-1392

retrieved

21 January 2018

Integrated detection and population-genetic analysis of SNPs and copy number variation

1 reference

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Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG1208-1392

retrieved

21 January 2018

Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes

1 reference

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Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG1208-1392

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21 January 2018

Large recurrent microdeletions associated with schizophrenia

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reference URL

https://api.crossref.org/works/10.1038%2FNG1208-1392

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21 January 2018

Obstetric complications and schizophrenia: historical and meta-analytic review

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21 January 2018

Copy-number variations associated with neuropsychiatric conditions

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reference URL

https://api.crossref.org/works/10.1038%2FNG1208-1392

retrieved

21 January 2018

Comparative genome hybridization suggests a role for NRXN1 and APBA2 in schizophrenia

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reference URL

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21 January 2018

Premorbid IQ in schizophrenia: a meta-analytic review

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21 January 2018

Endophenotypes in psychiatric genetics.

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21 January 2018

Intermediate phenotypes and genetic mechanisms of psychiatric disorders

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reference URL

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retrieved

21 January 2018

Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG1208-1392

retrieved

7 January 2021

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Rare chromosomal deletions and duplications increase risk of schizophrenia

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG1208-1392

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

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(Q57419525)

Phenotypic variations on the theme of CNVs

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