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...
| Autores principales: | , |
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| Formato: | Artículo |
| Lenguaje: | English |
| Publicado: |
UANL. Facultad de Medicina
2016
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| Acceso en línea: | http://eprints.uanl.mx/11709/1/S1665579616300503_S300_en.pdf |