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Query Trace: Hyperplasia and C4B[original query]

A rational, non-radioactive strategy for the molecular diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Gene 2013 Sep 526 (2): 239-45. Coeli-Lacchini Fernanda Borchers, Turatti Wendy, Elias Paula Conde Lamparelli, Elias Lucila Leico Kagohara, Martinelli Carlos Eduardo, Moreira Ayrton Custodio, Antonini Sonir Roberto, de Castro Margar Similar articles in PubMed
Association between copy number variation of complement component C4 and Graves' disease. Journal of biomedical science 2011 18 (1): 71. Liu Yu-Huei, Wan Lei, Chang Chwen-Tzuei, Liao Wen-Ling, Chen Wen-Chi, Tsai Yuhsin, Tsai Chang-Hai, Tsai Fuu-J Similar articles in PubMed
Linkage analysis of the C4A/C4B copy number variation and polymorphisms of the adjacent steroid 21-hydroxylase gene in a healthy population. Molecular immunology 2009 Aug 46 (13): 2623-9. Blaskó Bernadett, Bánlaki Zsófia, Gyapay Gabor, Pozsonyi Eva, Sasvári-Székely Mária, Rajczy Katalin, Füst George, Szilágyi Agn Similar articles in PubMed
Polymorphic markers in MHC class II/III region: a study on Italian patients with myasthenia gravis. Journal of the neurological sciences 2001 Sep 190 (1-2): 11-6. Franciotta D, Cuccia M, Dondi E, Piccolo G, Cosi Similar articles in PubMed