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Results: 2
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
Authors: ORDONEZSANCHEZ ML RAMIREZJIMENEZ S LOPEZGUTIERREZ AU RIBA L GAMBOACARDIEL S CERRILLOHINOJOSA M ALTAMIRANOBUSTAMANTE N CALZADALEON R ROBLESVALDES C MENDOZAMORFIN F TUSIELUNA MT
Citation: Ml. Ordonezsanchez et al., 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, Human genetics, 102(2), 1998, pp. 170-177
UNIPARENTAL DISOMY FOR CHROMOSOME-6 RESULTS IN STEROID 21-HYDROXYLASEDEFICIENCY - EVIDENCE OF DIFFERENT GENETIC MECHANISMS INVOLVED IN THEPRODUCTION OF THE DISEASE
Authors: LOPEZGUTIERREZ AU RIBA L ORDONEZSANCHEZ ML RAMIREZJIMENEZ S CERRILLOHINOJOSA M TUSIELUNA MT
Citation: Au. Lopezgutierrez et al., UNIPARENTAL DISOMY FOR CHROMOSOME-6 RESULTS IN STEROID 21-HYDROXYLASEDEFICIENCY - EVIDENCE OF DIFFERENT GENETIC MECHANISMS INVOLVED IN THEPRODUCTION OF THE DISEASE, Journal of Medical Genetics, 35(12), 1998, pp. 1014-1019
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