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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

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