A New 12q21 Deletion Syndrome: A Case Report and Literature Review

Diagnosis in children with physical and intellective anomalies is very challenging because of the wide spectrum of causes. Array-based comparative genomic hybridization (CGH) has acquired an important role in pediatric diagnostic work up. Interstitial deletion of the long arm of chromosome 12 are ra...

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Detalles Bibliográficos
Autores principales: Di Nora, Alessandra, De Costa, Greta, Di Mari, Alessia, Montemagno, Marco, Pavone, Vito, Pavone, Piero
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Georg Thieme Verlag KG 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9303074/
https://www.ncbi.nlm.nih.gov/pubmed/35873668
http://dx.doi.org/10.1055/s-0042-1748171

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9303074/
https://www.ncbi.nlm.nih.gov/pubmed/35873668
http://dx.doi.org/10.1055/s-0042-1748171

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