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Clinical and genetic aspects of Turner’s syndrome

Turner’s syndrome, or monosomy X, is defined as the total or partial loss of the second sex chromosome. The clinical phenotype is highly variable and includes short stature, gonadal dysgenesis, pterygium colli, cubitus valgus and low hairline. The variable expressivity of height and other physical...

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Detalles Bibliográficos
Autores principales:	Ibarra Ramírez, Marisol, Martínez de Villarreal, Laura Elia
Formato:	Artículo
Lenguaje:	inglés
Publicado:	UANL. Facultad de Medicina 2016
Acceso en línea:	http://eprints.uanl.mx/11709/1/S1665579616300503_S300_en.pdf

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