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You searched for: Author/Creator Chiang, Samuel C. C.

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1. Diagnostic challenges for a novel SH2D1A mutation associated with X‐linked lymphoproliferative disease. Issue 4 (29th January 2020)

2. Fatal Central Nervous System Lymphocytic Vasculitis after Treatment for Burkitt Lymphoma in a Patient with a SH2D1A Mutation. Issue 2 (February 2019)

3. Novel deep intronic and missense UNC13D mutations in familial haemophagocytic lymphohistiocytosis type 3. (14th May 2013)

4. Spectrum of Atypical Clinical Presentations in Patients with Biallelic PRF1 Missense Mutations. Issue 12 (16th July 2015)