A case report on atypical chromosomal variations in Turner syndrome
Abstract Background Turner syndrome (TS) is a common chromosomal abnormality caused by the complete or partial absence of one X chromosome. It affects approximately 1 in ~ 1,200 to 2,500 female births. In this case report, we examined the clinical details of a 21-year-old female for cytogenetic inve...
Αποθηκεύτηκε σε:
| Κύριοι συγγραφείς: | , , , , , |
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| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
BMC
2026-02-01
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| Σειρά: | Molecular Cytogenetics |
| Θέματα: | |
| Διαθέσιμο Online: | https://doi.org/10.1186/s13039-025-00745-0 |
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