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46,XX male disorder of sexual development
An individual’s sexual phenotype is usually determined by the presence or absence of the Y chromosome in the embryo’s karyotype, however, due to abnormal X/Y terminal exchange through male meiosis, a few individuals develop male genitalia in the absence of the Y chromosome. This case report presents...
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| Publicat a: | Clin Pediatr Endocrinol |
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| Autors principals: | , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
The Japanese Society for Pediatric Endocrinology
2020
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6958519/ https://ncbi.nlm.nih.gov/pubmed/32029971 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1297/cpe.29.43 |
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