Array Comparative Genomic Hybridization as a Diagnostic Tool for Syndromic Heart Defects-Reference-Cited by-同舟云学术

Array Comparative Genomic Hybridization as a Diagnostic Tool for Syndromic Heart Defects

Published:2010-05 Issue:5 Volume:156 Page:810-817.e4
ISSN:0022-3476
Container-title:The Journal of Pediatrics
language:en
Short-container-title:The Journal of Pediatrics

Author:

Breckpot Jeroen,Thienpont Bernard,Peeters Hilde,de Ravel Thomy,Singer Amihood,Rayyan Maissa,Allegaert Karel,Vanhole Christine,Eyskens Benedicte,Vermeesch Joris Robert,Gewillig Marc,Devriendt Koenraad

Funder

Agentschap voor Innovatie door Wetenschap en Technologie

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology, and Child Health

Reference35 articles.

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4. Submicroscopic chromosomal imbalances detected by array-CGH are a frequent cause of congenital heart defects in selected patients;Thienpont;Eur Heart J,2007

5. Whole-genome array-CGH screening in undiagnosed syndromic patients: old syndromes revisited and new alterations;Krepischi-Santos;Cytogenet Genome Res,2006

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