Congenital Generalized Hypomelanosis and Immunodeficiency in a Black Child
Author:
Publisher
Wiley
Subject
Dermatology,Pediatrics, Perinatology, and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1525-1470.2007.00371.x/fullpdf
Reference19 articles.
1. Chediak-Higashi Syndrome
2. Hermansky-Pudlak Syndrome and Chediak-Higashi Syndrome: Disorders of Vesicle Formation and Trafficking
3. Mutations in the Chediak-Higashi syndrome gene (CHS1) indicate requirement for the complete 3801 amino acid CHS protein
4. Clinical, Molecular, and Cell Biological Aspects of Chediak–Higashi Syndrome
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1. A novel single point mutation of the LYST gene in two siblings with different phenotypic features of Chediak Higashi syndrome;Pediatric Blood & Cancer;2011-02-04
2. Two Novel Mutations Identified in an African-American Child with Chediak-Higashi Syndrome;Case Reports in Medicine;2010
3. Disorders of pigmentation;Weedon's Skin Pathology;2010
4. The Diagnosis;Differential Diagnosis for the Dermatologist;2008
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