Skin lesions in a boy with X-linked lymphoproliferative disorder: comparison of 5 SH2D1A deletion cases. [electronic resource]
Producer: 20120327Description: e523-8 p. digitalISSN:- 1098-4275
- Adolescent
- Adult
- Anemia, Aplastic -- diagnosis
- Child
- Child, Preschool
- Chromosome Deletion
- Chromosomes, Human, X -- genetics
- Comorbidity
- Exons -- genetics
- Histiocytic Sarcoma -- diagnosis
- Humans
- Infectious Mononucleosis -- diagnosis
- Intracellular Signaling Peptides and Proteins -- genetics
- Longitudinal Studies
- Lymphoproliferative Disorders -- diagnosis
- Male
- Membrane Proteins -- genetics
- Nerve Tissue Proteins
- Peripheral Blood Stem Cell Transplantation
- Phenotype
- Scleroderma, Localized -- diagnosis
- Signaling Lymphocytic Activation Molecule Associated Protein
- Skin Diseases, Vesiculobullous -- diagnosis
- Tenascin
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Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
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