20p12.3 microdeletion predisposes to Wolff-Parkinson-White syndrome with variable neurocognitive deficits.
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The genetics of attention deficit/hyperactivity disorder in adults, a reviewGene regulatory networks in cardiac conduction system development20p12.3 deletion is rare cause of syndromic cleft palate: case report and review of literatureThe cardiac conduction systemNotch signaling regulates murine atrioventricular conduction and the formation of accessory pathways.Assessment of atrial fibrillation and vulnerability in patients with Wolff-Parkinson-White syndrome using two-dimensional speckle tracking echocardiography.Defective Tbx2-dependent patterning of the atrioventricular canal myocardium causes accessory pathway formation in miceCopy number variation in human health, disease, and evolution.Cryptic genomic rearrangements in three patients with 46,XY disorders of sex development.Genomic disorders ten years on.BMP signaling in congenital heart disease: new developments and future directions.Origin and development of the atrioventricular myocardial lineage: insight into the development of accessory pathways.Electrophysiological patterning of the heart.Tachyarrhythmias and catheter ablation in adult congenital heart disease.Development and Function of the Cardiac Conduction System in Health and Disease.Pharmacological and non-pharmacological therapy for arrhythmias in the pediatric population: EHRA and AEPC-Arrhythmia Working Group joint consensus statement.Monoallelic BMP2 Variants Predicted to Result in Haploinsufficiency Cause Craniofacial, Skeletal, and Cardiac Features Overlapping Those of 20p12 Deletions.A heterozygous microdeletion of 20p12.2-3 encompassing PROKR2 and BMP2 in a patient with congenital hypopituitarism and growth hormone deficiency.
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20p12.3 microdeletion predisposes to Wolff-Parkinson-White syndrome with variable neurocognitive deficits.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on 23 September 2008
@en
vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
20p12.3 microdeletion predispo ...... iable neurocognitive deficits.
@en
20p12.3 microdeletion predispo ...... iable neurocognitive deficits.
@nl
type
label
20p12.3 microdeletion predispo ...... iable neurocognitive deficits.
@en
20p12.3 microdeletion predispo ...... iable neurocognitive deficits.
@nl
prefLabel
20p12.3 microdeletion predispo ...... iable neurocognitive deficits.
@en
20p12.3 microdeletion predispo ...... iable neurocognitive deficits.
@nl
P2093
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20p12.3 microdeletion predispo ...... iable neurocognitive deficits.
@en
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A C Chinault
E K Brundage
I Hansmann
J A Towbin
J F Martin
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P304
P356
10.1136/JMG.2008.061002
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P577
2008-09-23T00:00:00Z