Case report: Molecular analysis of a 47,XY,+21/46,XX chimera using SNP microarray and review of literature

Chimerism is a very rare genetic finding in human. Most reported cases have a chi 46,XX/46,XY karyotype. Only three non-twin cases carrying both trisomy 21 and a normal karyotype have been reported, including two cases with a chi 47,XY,+21/46,XX karyotype and a case with a chi 47,XX,+21/46,XY karyot...

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Detalles Bibliográficos
Autores principales: Charalsawadi, Chariyawan, Jaruratanasirikul, Somchit, Hnoonual, Areerat, Chantarapong, Aussanai, Sangmanee, Pornsiri, Trongnit, Sasipong, Jinawath, Natini, Limprasert, Pornprot
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9709885/
https://www.ncbi.nlm.nih.gov/pubmed/36468027
http://dx.doi.org/10.3389/fgene.2022.802362

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9709885/
https://www.ncbi.nlm.nih.gov/pubmed/36468027
http://dx.doi.org/10.3389/fgene.2022.802362

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