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Optimising management in Turner syndrome: from infancy to adult transfer
Turner syndrome can be defined as loss or abnormality of the second X chromosome in at least one cell line in a phenotypic female. The condition occurs in approximately 1 in every 2000 live female births,1 so that in the UK the prevalence for any year of life is in the region of 200 girls. The condi...
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| Main Authors: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BMJ Group
2006
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2082783/ https://ncbi.nlm.nih.gov/pubmed/16714725 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/adc.2003.035907 |
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