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Histiocytosis with joint contractures...

Histiocytosis with joint contractures and sensorineural deafness

December 31, 2014

Latest Research

A novel homozygous frame-shift mutation in the SLC29A3 gene: a new case report and review of literature
A novel start-loss mutation of the SLC29A3 gene in a consanguineous family with H syndrome: clinical characteristics, in silico analysis and literature review
A Rare Autoimmune Disease Detected in the Differential Diagnosis of Immunodeficiency: Histiocytosis-lymphadenopathy Plus Syndrome
Accelerated coronary atherosclerosis and H syndrome
An Egyptian family with H syndrome due to a novel mutation in SLC29A3 illustrating overlapping features with pigmented hypertrichotic dermatosis with insulin-dependent diabetes and Faisalabad histiocytosis

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