Phenotypic variability in siblings with Farber disease. | J Pediatr;104(3): 406-9, 1984 Mar. | MEDLINE

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Phenotypic variability in siblings with Farber disease.

Antonarakis, S E; Valle, D; Moser, H W; Moser, A; Qualman, S J; Zinkham, W H.

J Pediatr ; 104(3): 406-9, 1984 Mar.

Article in En | MEDLINE | ID: mdl-6423791

Subject(s)

Amidohydrolases/deficiency; Sphingolipidoses/genetics; Ceramidases; Clinical Enzyme Tests; Female; Femur Head/diagnostic imaging; Genetic Variation; Humans; Humerus/diagnostic imaging; Infant; Male; Phenotype; Radiography; Sphingolipidoses/diagnosis

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Collection: 01-internacional Database: MEDLINE Main subject: Sphingolipidoses / Amidohydrolases Type of study: Diagnostic_studies Limits: Female / Humans / Infant / Male Language: En Journal: J Pediatr Year: 1984 Document type: Article Country of publication: United States

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Collection: 01-internacional Database: MEDLINE Main subject: Sphingolipidoses / Amidohydrolases Type of study: Diagnostic_studies Limits: Female / Humans / Infant / Male Language: En Journal: J Pediatr Year: 1984 Document type: Article Country of publication: United States