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
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
Authors:
TUSIELUNA MT
RAMIREZJIMENEZ S
ORDONEZSANCHEZ ML
CABELLOVILLEGAS J
ALTAMIRANOBUSTAMANTE N
CALZADALEON R
ROBLESVALDES C
MENDORZAMORFIN F
MENDEZ JP
TERANGARCIA M
Citation: Mt. Tusieluna et al., LOW-FREQUENCY OF DELETION ALLELES IN PATIENTS WITH STEROID 21-HYDROXYLASE DEFICIENCY IN A MEXICAN POPULATION, Human genetics, 98(3), 1996, pp. 376-379