Prenatal Diagnosis of Walker--Warburg Syndrome Using Single Nucleotide Polymorphism Array: A Clinical Experience from Three Related Palestinian Families with Congenital Hydrocephalus.
Autor: | Abumansour, Iman S., Al Sulmi, Eman, Chodirker, Bernard N., Hunt, Jennifer C. |
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Zdroj: | American Journal of Perinatology Reports; 2015, Vol. 5 Issue 2, pe116-e120, 5p |
Databáze: | Complementary Index |
Externí odkaz: |