(Q38160092)

30 August 2017

title

Array CGH as a first-tier test for neonates with congenital heart disease (English)

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Constantinos Chrysostomou

30 August 2017

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3

object named as

Constantinos Chrysostomou

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30 August 2017

Kristine K Bachman

1

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30 August 2017

Stephanie J DeWard

2

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30 August 2017

Ricardo Munoz

4

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30 August 2017

Suneeta Madan-Khetarpal

5

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30 August 2017

publication date

6 November 2013

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30 August 2017

published in

Cardiology in the Young

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30 August 2017

volume

25

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30 August 2017

issue

1

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30 August 2017

page(s)

115-122

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

30 August 2017

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Submicroscopic chromosomal imbalances detected by array-CGH are a frequent cause of congenital heart defects in selected patients

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7 January 2021

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A novel microdeletion at 16p11.2 harbors candidate genes for aortic valve development, seizure disorder, and mild mental retardation

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7 January 2021

10.1017/S1047951113001868

Identifiers

DOI

1 reference

30 August 2017

1 reference