Currarino Syndrome in Two Moroccan Siblings with Inherited 7q36 Deletion due to Maternal t(7;21)(q36;p11)mat: A Case Report.
| Autor: | El Amrani, Zhour, Natiq, Abdelhafid, Sbiti, Aziza, Ratbi, Ilham, Liehr, Thomas, Sefiani, Abdelaziz, Sahli, Maryem |
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| Zdroj: | Molecular Syndromology; 2024, Vol. 15 Issue 2, p125-129, 5p |
| Databáze: | Complementary Index |
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