Related Experiment Videos

Lymphoedema in hereditary recurrent cholestasis from birth

O Aagenaes, H Sigstad, R Bjorn-Hansen

Archives of Disease in Childhood

|October 1, 1970

Summary

No abstract available in PubMed .

Related Concept Videos

Articles linked to this work by shared authors, journal, and citation graph.

Mapping of the locus for cholestasis-lymphedema syndrome (Aagenaes syndrome) to a 6.6-cM interval on chromosome 15q.

American journal of human genetics·2000

Homozygous mutation (A228T) in the 5alpha-reductase type 2 gene in a boy with 5alpha-reductase deficiency: genotype-phenotype correlations.

American journal of medical genetics·1998

Autosomal glycogenosis of liver and muscle due to phosphorylase kinase deficiency is caused by mutations in the phosphorylase kinase beta subunit (PHKB).

Human molecular genetics·1997

[Familial hypercholesterolemia in children. A management program. Procedures for diagnosis and treatment in our pediatric departments].

Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke·1995

The effect of 8 years of strict glycaemic control on peripheral nerve function in IDDM patients: the Oslo Study.

Diabetologia·1994

[Hereditary intrahepatic cholestasis with lymphedema--Aagenaes syndrome].

Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke·1993

See all related articles