Heterotaxy in a Fetus with Prenatally Diagnosed 15q11.2 Microdeletion Syndrome.
Autor: | Wilson, Patrick L., Rubenstein, Abby, Xainfu Wang, Shibo Li, Porter, Blake |
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Zdroj: | Journal of the Oklahoma State Medical Association; Mar/Apr2024, Vol. 117 Issue 2, p55-59, 5p |
Databáze: | Complementary Index |
Externí odkaz: |