Genetic and phenotypic continuum of HOXA genes: A case with double HOXA9/HOXA13 mutations

The HOXA genes cluster plays a key role in embryologic development. Mutations in HOXA genes have been linked to different human phenotypes, including developmental delay, limb anomalies, and urogenital malformations. The present study reported a clinical and genetic investigation of a female patient...

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Detalles Bibliográficos
Autores principales: Jaouadi, Hager, Theron, Alexis, Norscini, Giulia, Avierinos, Jean-François, Zaffran, Stéphane
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2023
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9936258/
https://www.ncbi.nlm.nih.gov/pubmed/36734258
http://dx.doi.org/10.3892/mmr.2023.12946

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9936258/
https://www.ncbi.nlm.nih.gov/pubmed/36734258
http://dx.doi.org/10.3892/mmr.2023.12946

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