Applying deep DNA sequencing to common, complex pediatric traits.

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Applying deep DNA sequencing to common, complex pediatric traits.

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2012 nî lūn-bûn

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2012年の論文

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2012年学术文章

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2012年学术文章

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2012年学术文章

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2012年学术文章

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2012年学术文章

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2012年學術文章

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2012年學術文章

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2012年學術文章

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Applying deep DNA sequencing to common, complex pediatric traits.

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Applying deep DNA sequencing to common, complex pediatric traits.

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Applying deep DNA sequencing to common, complex pediatric traits.

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Applying deep DNA sequencing to common, complex pediatric traits.

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Applying deep DNA sequencing to common, complex pediatric traits.

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Applying deep DNA sequencing to common, complex pediatric traits.

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P1476

Applying deep DNA sequencing to common, complex pediatric traits

@en

P2093

Jeffrey C Murray

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P2860

Assessing public attitudes on the retention and use of residual newborn screening blood samples: a focus group study.

Non-invasive prenatal measurement of the fetal genome

Rapid whole-genome sequencing for genetic disease diagnosis in neonatal intensive care units.

The human microbiome and its potential importance to pediatrics.

Incidental medical information in whole-exome sequencing.

The impact of genomics on pediatric research and medicine.

Noninvasive whole-genome sequencing of a human fetus.

Single ABCA3 mutations increase risk for neonatal respiratory distress syndrome.

Clan genomics and the complex architecture of human disease.

The Centers for Mendelian Genomics: a new large-scale initiative to identify the genes underlying rare Mendelian conditions.

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e1677-8

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scholarly article

P356

10.1542/PEDS.2012-2870

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English

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130

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P50

John M Dagle

P577

2012-11-19T00:00:00Z

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23166345

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3507258

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