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Diagnostic and clinical utility of exome sequencing and chromosomal microarray in children with GDD/iD: a meta-analysis

Background Global developmental delay/intellectual disability (GDD/ID) is among the most common neurodevelopmental disorders, with up to half of cases are attributed to genetic factors. Chromosome microarray (CMA) has traditionally been the primary genetic test for idiopathic GDD/ID. However, whole...

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Hlavní autoři: Maliwan Tengsujaritkul, Orawan Louthrenoo, Narueporn Likhitweerawong, Nonglak Boonchooduang, Manit Srisurapanont
Médium: Artigo
Jazyk:Inglês
Vydáno: Taylor & Francis Group 2026-12-01
Edice:Annals of Medicine
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On-line přístup:https://www.tandfonline.com/doi/10.1080/07853890.2025.2609424
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