A Novel 3q29 Deletion in Association With Developmental Delay and Heart Malformation—Case Report With Literature Review
3q29 deletion syndrome is a rare disorder, causing a complex phenotype. Clinical features are variable and relatively non-specific. Our report aims to present an atypical, de novo deletion in chromosome band 3q29 in a preschool boy, first child of healthy non-consanguineous parents, presenting a par...
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| Hoofdauteurs: | , , , , , , , |
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| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Frontiers Media S.A.
2019-07-01
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| Reeks: | Frontiers in Pediatrics |
| Onderwerpen: | |
| Online toegang: | https://www.frontiersin.org/article/10.3389/fped.2019.00270/full |
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