Interstitial 20p13 microdeletion including PRNP and adjacent genes in a fetus with congenital abnormalities—First case report

We present a prenatal case with congenital anomalies that revealed a 759 kb microdeletion at 20p13 possibly implicating PRNP and adjacent genes.

Detalles Bibliográficos
Autores principales: Onur, Pelin, Shaver, Mary, Iqbal, Mohammed Anwaruddin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8142463/
https://www.ncbi.nlm.nih.gov/pubmed/34084500
http://dx.doi.org/10.1002/ccr3.4082

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8142463/
https://www.ncbi.nlm.nih.gov/pubmed/34084500
http://dx.doi.org/10.1002/ccr3.4082

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