| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 4168209 | The Journal of Pediatrics | 2010 | 12 Pages |
Abstract
Molecular karyotyping yields an etiological diagnosis in at least 18% of patients with a syndromic CHD. Higher resolution evaluation results in an increasing number of variants of unknown significance.
Keywords
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Perinatology, Pediatrics and Child Health
Authors
Jeroen MD, Bernard PhD, Hilde MD, PhD, Thomy MD, PhD, Amihood MD, Maissa MD, Karel MD, PhD, Prof, Christine MD, PhD, Prof, Benedicte MD, PhD, Prof, Joris Robert PhD, Prof, Marc MD, PhD, Prof, Koenraad MD, PhD, Prof,