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Molecular genetic analysis of patients carrying steroid 21-hydroxylase deficiency in the Mexican population: identification of possible new mutations and high prevalence of apparent germ-line mutations.
Hum Genet. 1998 Feb;102(2):170-7. doi: 10.1007/s004390050672.
Hum Genet. 1998.
PMID: 9580109
Uniparental disomy for chromosome 6 results in steroid 21-hydroxylase deficiency: evidence of different genetic mechanisms involved in the production of the disease.
López-Gutiérrez AU, Riba L, Ordoñez-Sánchez ML, Ramírez-Jiménez S, Cerrillo-Hinojosa M, Tusié-Luna MT.
López-Gutiérrez AU, et al.
J Med Genet. 1998 Dec;35(12):1014-9. doi: 10.1136/jmg.35.12.1014.
J Med Genet. 1998.
PMID: 9863599
Free PMC article.
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