Prenatal Diagnosis of Walker–Warburg Syndrome Using Single Nucleotide Polymorphism Array: A Clinical Experience from Three Related Palestinian Families with Congenital Hydrocephalus

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Location: Deutsche Nationalbibliothek Frankfurt am Main

Extent: Online-Ressource

Language: Englisch

Bibliographic citation: Prenatal Diagnosis of Walker–Warburg Syndrome Using Single Nucleotide Polymorphism Array: A Clinical Experience from Three Related Palestinian Families with Congenital Hydrocephalus ; volume:05 ; number:02 ; year:2015 ; pages:e116-e120
AJP reports ; 05, Heft 02 (2015), e116-e120

Contributor: Abumansour, Iman S.
Al Sulmi, Eman
Chodirker, Bernard N.
Hunt, Jennifer C.

DOI: 10.1055/s-0035-1549298

URN: urn:nbn:de:101:1-2019040913073217926173

Rights: Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 14.08.2025, 10:48 AM CEST

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Abumansour, Iman S.
Al Sulmi, Eman
Chodirker, Bernard N.
Hunt, Jennifer C.

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Prenatal Diagnosis of Walker–Warburg Syndrome Using Single Nucleotide Polymorphism Array: A Clinical Experience from Three Related Palestinian Families with Congenital Hydrocephalus

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