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Genetic Sophistication of Human Complement Components C4A and C4B and RP-C4-CYP21-TNX (RCCX) Modules in the Major Histocompatibility Complex - ScienceDirect
High-Throughput Screening for CYP21A1P-TNXA/TNXB Chimeric Genes Responsible for Ehlers-Danlos Syndrome in Patients with Congenit
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Human Complement Components C4A and C4B Genetic Diversities: Complex Genotypes and Phenotypes - Chung - 2005 - Current Protocols in Immunology - Wiley Online Library
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Three common arrangements of the RCCX module. Monomodular, bimodular,... | Download Scientific Diagram
Modular Variations of the Human Major Histocompatibility Complex Class III Genes for Serine/Threonine Kinase RP, Complement Comp
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The sophisticated genetic diversities of human complement component C4 and RCCX modules in systemic lupus erythematosus and congenital adrenal hyperplasia | Semantic Scholar
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Congenital adrenal hyperplasia due to two rare CYP21A2 variant alleles, including a novel attenuated CYP21A1P/CYP21A2 chimera - Lao - Molecular Genetics & Genomic Medicine - Wiley Online Library
Both Positive and Negative Selection Pressures Contribute to the Polymorphism Pattern of the Duplicated Human CYP21A2 Gene | PLOS ONE
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PDF] Intraspecific Evolution of Human RCCX Copy Number Variation Traced by Haplotypes of the CYP21A2 Gene | Semantic Scholar
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Modular Variations of the Human Major Histocompatibility Complex Class III Genes for Serine/Threonine Kinase RP, Complement Component C4, Steroid 21-Hydroxylase CYP21, and Tenascin TNX (the RCCX Module): A MECHANISM FOR GENE DELETIONS
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Organization of RCCX module and Copy Number Variations at chromosome... | Download Scientific Diagram
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Diploid combinations of the RCCX modules in the Caucasian population.... | Download Scientific Diagram
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Fine-tuned characterization of RCCX copy number variants and their relationship with extended MHC haplotypes | Genes & Immunity
RCCX modules: Bimodular haplotype (upper) and a three modular haplotype... | Download Scientific Diagram
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The sophisticated genetic diversities of human complement component C4 and RCCX modules in systemic lupus erythematosus and congenital adrenal hyperplasia | Semantic Scholar
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Mapping of a de novo unequal crossover causing a deletion of the steroid 21-hydroxylase (CYP21A2) gene and a non-functional hybrid tenascin-X (TNXB) gene | Journal of Medical Genetics
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EMQN best practice guidelines for molecular genetic testing and reporting of 21-hydroxylase deficiency | European Journal of Human Genetics
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Modular Variations of the Human Major Histocompatibility Complex Class III Genes for Serine/Threonine Kinase RP, Complement Component C4, Steroid 21-Hydroxylase CYP21, and Tenascin TNX (the RCCX Module): A MECHANISM FOR GENE DELETIONS
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A unique haplotype of RCCX copy number variation: from the clinics of congenital adrenal hyperplasia to evolutionary genetics | European Journal of Human Genetics
GeNeViSTA Challenges of Molecular Analysis of Congenital Adrenal Hyperplasia Caused Due to Steroid 21 Hydroxylase Deficiency
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C4B null alleles are not associated with genetic polymorphisms in the adjacent gene CYP21A2in autism | BMC Medical Genetics | Full Text
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