| 1 | C4A,C4B, CYP21A2, CYP21A1P
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| High variability of CYP21 gene rearrangements in Spanish patients with classic form of congenital adrenal hyperplasia.
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| Lobato MN, Aledo R, Meseguer A.
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| Hum Hered 48 : 216-225. 1998
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| 2 | ATF6B, CYP21A1P, TNXB
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| Alternate promoters and alternate splicing of human tenascin-X, a gene with 5' and 3' ends buried in other genes.
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| Speek M, et al.
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| Hum Mol Genet 5 : 1749-1758. 1996
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| 3 | CYP21A2, CYP21A1P
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| Detection of steroid 21-hydroxylase alleles using gene-specific PCR and a multiplexed ligation detection reaction.
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| Day DJ, Speiser PW, White PC, Barany F.
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| Genomics 29 : 152-162. 1995
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| 4 | CYP21A2, CYP21A1P
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| Gene conversions and unequal crossovers between CYP21 (steroid 21-hydroxylase gene) and CYP21P involve different mechanisms.
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| Tusie-Luna MT, White PC.
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| Proc Natl Acad Sci U S A 92 : 10796-10800. 1995
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| 5 | CYP21A1P, CYP21A2
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| R339H and P453S: CYP21 mutations associated with nonclassic steroid 21-hydroxylase deficiency that are not apparent gene conversions.
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| Helmberg A, Tusie-Luna MT, Tabarelli M, Kofler R, White PC.
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| Mol Endocrinol 6(8):1318-22 1992
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| 6 | CYP21A2, CYP21A1P
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| Genetic mapping of the 21-hydroxylase locus : estimatiom of small recombination frequencies.
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| Aston CE, Sherman SL, Morton NE, Speiser PW, New MI.
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| Am J Hum Genet 43 : 304-310. 1988
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