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Results: 1-6 |
Results: 6
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
ANALYSIS OF THE GLUCOKINASE GENE IN MEXICAN FAMILIES DISPLAYING EARLY-ONSET NON-INSULIN-DEPENDENT DIABETES-MELLITUS INCLUDING MODY FAMILIES
Authors: DELBOSQUEPLATA L GARCIAGARCIA E RAMIREZJIMENEZ S CABELLOVILLEGAS J RIBA L GOMEZLEON A VEGAHERNANDEZ G ALTAMIRANOBUSTAMANTE N CALZADALEON R ROBLESVALDES C MENDOZAMORFIN F CURIELPEREZ O TUSIELUNA MT
Citation: L. Delbosqueplata et al., ANALYSIS OF THE GLUCOKINASE GENE IN MEXICAN FAMILIES DISPLAYING EARLY-ONSET NON-INSULIN-DEPENDENT DIABETES-MELLITUS INCLUDING MODY FAMILIES, American journal of medical genetics, 72(4), 1997, pp. 387-393
LOW-FREQUENCY OF DELETION ALLELES IN PATIENTS WITH STEROID 21-HYDROXYLASE DEFICIENCY IN A MEXICAN POPULATION
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
GENE CONVERSIONS AND UNEQUAL CROSSOVERS BETWEEN CYP21 (STEROID 21-HYDROXYLASE GENE) AND CYP21P INVOLVE DIFFERENT MECHANISMS
Authors: TUSIELUNA MT WHITE PC
Citation: Mt. Tusieluna et Pc. White, GENE CONVERSIONS AND UNEQUAL CROSSOVERS BETWEEN CYP21 (STEROID 21-HYDROXYLASE GENE) AND CYP21P INVOLVE DIFFERENT MECHANISMS, Proceedings of the National Academy of Sciences of the United Statesof America, 92(23), 1995, pp. 10796-10800
MUTATIONS IN STEROID 21-HYDROXYLASE (CYP21)
Authors: WHITE PC TUSIELUNA MT NEW MI SPEISER PW
Citation: Pc. White et al., MUTATIONS IN STEROID 21-HYDROXYLASE (CYP21), Human mutation, 3(4), 1994, pp. 373-378
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