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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

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