Interstitial Deletion of 3q21 in a Kuwaiti Child with Multiple Congenital Anomalies—Expanding the Phenotype

Interstitial deletions in the long arm of chromosome 3, although relatively rare, have previously been reported to be associated with several congenital anomalies and developmental delays. Around 11 individuals with interstitial deletion spanning the region 3q21 were reported to have overlapping phe...

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Detalles Bibliográficos
Autores principales: Almoosawy, Noor, Albaghli, Fawaz, Al-Balool, Haya H., Fathi, Hanan, Zakaria, Waleed A., Ayed, Mariam, Alsharhan, Hind
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10298411/
https://www.ncbi.nlm.nih.gov/pubmed/37372405
http://dx.doi.org/10.3390/genes14061225

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10298411/
https://www.ncbi.nlm.nih.gov/pubmed/37372405
http://dx.doi.org/10.3390/genes14061225

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