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A parthenogenetic maternal and double paternal contribution to an ovotesticular disorder of sex development
BACKGROUND: An ovotesticular disorder of sex development (OT-DSD) was rarely found in human. The mechanism causing such condition is poorly understood. We hereby reported a 11-year-old child with OT-DSD and a karyotype 46,XX/46,XY, a single maternal and double paternal genetic contribution to the pa...
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Main Authors: | , , , , , , , , , |
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Formato: | Artigo |
Idioma: | Inglês |
Publicado em: |
BioMed Central
2014
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Assuntos: | |
Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3974030/ https://ncbi.nlm.nih.gov/pubmed/24581244 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1755-8166-7-16 |
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