Y Chromosome Material in Turner Syndrome

Background Turner Syndrome (TS) is a frequently identified chromosomal disease in humans characterized by short stature, sexual infantilism, streak gonads, primary amenorrhea, and a number of somatic anomalies. Approximately 55% of TS individuals have a nonmosaic 45,X karyotype. In addition, a cell...

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Detalles Bibliográficos
Autores principales: Akcan, Abdullah Baris, Boduroğlu, Osman K
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2021
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8628189/
https://www.ncbi.nlm.nih.gov/pubmed/34868795
http://dx.doi.org/10.7759/cureus.19977

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8628189/
https://www.ncbi.nlm.nih.gov/pubmed/34868795
http://dx.doi.org/10.7759/cureus.19977

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