(Q56232661)

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Editorial comment on "Whole exome sequencing identifies compound heterozygous mutations in WDR62 in siblings with recurrent polymicrogyria"

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Editorial comment on "Whole exome sequencing identifies compound heterozygous mutations in WDR62 in siblings with recurrent polymicrogyria" (English)

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1

Leslie G Biesecker

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language of work or name

English

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publication date

September 2011

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published in

American Journal of Medical Genetics

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volume

155A

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issue

9

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page(s)

2069-70

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cites work

Making a definitive diagnosis: successful clinical application of whole exome sequencing in a child with intractable inflammatory bowel disease

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reference URL

https://api.crossref.org/works/10.1002%2FAJMG.A.34183

retrieved

21 January 2018

Identifiers

DOI

10.1002/AJMG.A.34183

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PubMed publication ID

21834027

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(Q56232661)

Editorial comment on "Whole exome sequencing identifies compound heterozygous mutations in WDR62 in siblings with recurrent polymicrogyria"

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