A 15q25.2 microdeletion phenotype for premature ovarian failure in a Chinese girl: a case report and review of literature

BACKGROUND: Proximal microdeletions on chromosome 15q25.2 are very rare, and are associated with neurodevelopmental delay, inguinal hernia, chest deformities, and anemia. The minimum length missed so far is 1.4 Mb. However, there were no cases reported till date on microdeletions at position q25.2 o...

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Detalles Bibliográficos
Autores principales: Chen, Zhen, Chen, Hong, Yuan, Ke, Wang, Chunlin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7487592/
https://www.ncbi.nlm.nih.gov/pubmed/32894148
http://dx.doi.org/10.1186/s12920-020-00787-w

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7487592/
https://www.ncbi.nlm.nih.gov/pubmed/32894148
http://dx.doi.org/10.1186/s12920-020-00787-w

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