Prenatal Diagnosis of Combined Maternal 4q Interstitial Deletion and Paternal 15q Microduplication

The 4q deletion syndrome is a well-known rare genetic condition caused by partial, terminal, or interstitial deletion in the long arm (q) of chromosome 4. The phenotype of this syndrome shows a broad spectrum of clinical manifestations due to the great variability in the size and location of the del...

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Detalles Bibliográficos
Autores principales: Libotte, Francesco, Fabiani, Marco, Margiotti, Katia, Viola, Antonella, Mesoraca, Alvaro, Giorlandino, Claudio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8536159/
https://www.ncbi.nlm.nih.gov/pubmed/34681020
http://dx.doi.org/10.3390/genes12101626

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8536159/
https://www.ncbi.nlm.nih.gov/pubmed/34681020
http://dx.doi.org/10.3390/genes12101626

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