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Article

Hydrops fetalis: manifestation in lysosomal storage diseases including Farber disease

25 Mar 1997

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 9128814
DOI: 10.1007/s004310050603

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Related research

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Click a neighbor to travelStep 1 · 12 closest

Hydrops fetalis: manifestation in lysosomal storage diseases including Farber diseasePMID 9128814Read ↗

Hydrops Fetalis: Lysosomal Storage Disorders In ExtremisSemantic proximity Read ↗

Lysosomal storage disorders as an etiology of nonimmune hydrops fetalis: A systematic review.Semantic proximity Read ↗

Hydrops Fetalis Caused by α-Thalassemia: An Emerging Health Care ProblemSemantic proximity Read ↗

PRKAG2 -Related Lethal Congenital Glycogen Storage Disease of the Heart as Rare Cause of Fetal Hydrops With Bradycardia and Cardiomyopathy: Clinical Report and Literature Review.Semantic proximity Read ↗

Lysosomal storage disorders in nonimmune hydrops fetalis diagnosed by exome sequencingSemantic proximity Read ↗

Fetal Hydrops: Genetic Dissection of an Unspecific Sonographic Finding—A Comprehensive ReviewSemantic proximity Read ↗

Nonimmune hydrops fetalis: identifying the underlying genetic etiologySemantic proximity Read ↗

Investigation of lysosomal storage diseases in nonimmune hydrops fetalisSemantic proximity Read ↗

Gaucher Disease in Fetus: The Usual and the Unusual Presentations in a FamilySemantic proximity Read ↗

Angelman syndrome: mimicking conditions and phenotypes.Semantic proximity Read ↗

Etiology of non‐immune hydrops fetalis: An updateSemantic proximity Read ↗

Lysosomal storage diseases in non-immune hydrops fetalis pregnancies.Semantic proximity Read ↗

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