Deletion of b1/b3 shows risk for expanse of Yq microdeletion in male offspring: Case report of novel Y chromosome variations

RATIONALE: This study aimed to report 1 family case with novel Y chromosome structural variations by an established next-generation sequencing (NGS) method using unique STSs. PATIENT CONCERNS: The case studied was from a family with a father and son (the proband). G-band staining was used for karyot...

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Detalles Bibliográficos
Autores principales: Liu, Xiangyin, Zhang, Hongguo, Yu, Yang, Fei, Jia, Jiang, Yuting, Liu, Ruizhi, Wang, Ruixue, Zhang, Guirong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2020
Materias:
7300
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7489624/
https://www.ncbi.nlm.nih.gov/pubmed/32925763
http://dx.doi.org/10.1097/MD.0000000000022124

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7489624/
https://www.ncbi.nlm.nih.gov/pubmed/32925763
http://dx.doi.org/10.1097/MD.0000000000022124

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