Mejstríková, Ester <br/><br/>
Skin lesions in a boy with X-linked lymphoproliferative disorder: comparison of 5 SH2D1A deletion cases.  [electronic resource] 

 -  Pediatrics  Feb 2012 
 - e523-8 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1098-4275 
<br/><br/><label>Standard No.: </label>10.1542/peds.2011-0870  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Anemia, Aplastic--diagnosis<br/>Child<br/>Child, Preschool<br/>Chromosome Deletion<br/>Chromosomes, Human, X--genetics<br/>Comorbidity<br/>Exons--genetics<br/>Histiocytic Sarcoma--diagnosis<br/>Humans<br/>Infectious Mononucleosis--diagnosis<br/>Intracellular Signaling Peptides and Proteins--genetics<br/>Longitudinal Studies<br/>Lymphoproliferative Disorders--diagnosis<br/>Male<br/>Membrane Proteins--genetics<br/>Nerve Tissue Proteins<br/>Peripheral Blood Stem Cell Transplantation<br/>Phenotype<br/>Scleroderma, Localized--diagnosis<br/>Signaling Lymphocytic Activation Molecule Associated Protein<br/>Skin Diseases, Vesiculobullous--diagnosis<br/>Tenascin