Prenatal diagnosis of familial 46,X,del(X)(q27.1) with an Xq27.1-q28 deletion and an Xp22.33 microduplication in an asymptomatic mother carrier
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| Médium: | Článek |
| Jazyk: | English |
| Vydáno: |
Elsevier
2025-03-01
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| Edice: | Taiwanese Journal of Obstetrics & Gynecology |
| On-line přístup: | http://www.sciencedirect.com/science/article/pii/S1028455925000440 |