Veronique Tardy

Summary

Affiliation: Hospices Civils de Lyon
Country: France

Publications

  1. ncbi request reprint Gene symbol: CYP21A2. Disease: steroid 21-hydroxylase deficiency
    Veronique Tardy
    Laboratoire de Biologie Moleculaire, Hopital Debrousse, Lyon, France
    Hum Genet 119:363. 2006
  2. ncbi request reprint Gene symbol: CYP21A2
    Veronique T V Tardy
    Laboratoire de Biologie Moleculaire, Hopital Debrousse, 29 rue Soeur Bouvier, Lyon Cedex, France
    Hum Genet 121:293. 2007
  3. ncbi request reprint Gene symbol: CYP21A2
    Veronique T V Tardy
    Laboratoire de Biologie Moleculaire, Hopital Debrousse, 29 rue Soeur Bouvier, Lyon Cedex, France
    Hum Genet 121:292. 2007
  4. ncbi request reprint Gene symbol: CYP21A2
    Veronique T V Tardy
    Laboratoire de Biologie Moleculaire, Hopital Debrousse, 29 rue Soeur Bouvier, Lyon Cedex, France
    Hum Genet 121:292-3. 2007
  5. ncbi request reprint Gene symbol: CYP21A2
    Veronique T V Tardy
    Laboratoire de Biologie Moleculaire, Hopital Debrousse, 29 rue Soeur Bouvier, Lyon Cedex, France
    Hum Genet 121:293. 2007
  6. ncbi request reprint Gene symbol: CYP21A2
    Veronique T V Tardy
    Hopital Debrousse, Laboratoire de Biologie Moleculaire, 29 rue Soeur Bouvier, Lyon Cedex, France
    Hum Genet 121:293-4. 2007
  7. ncbi request reprint Gene symbol: CYP21A2
    Veronique T V Tardy
    Hopital Debrousse, Laboratoire de Biologie Moleculaire, 29 rue Soeur Bouvier, Lyon Cedex, France
    Hum Genet 121:294. 2007
  8. doi request reprint Phenotype-genotype correlations of 13 rare CYP21A2 mutations detected in 46 patients affected with 21-hydroxylase deficiency and in one carrier
    V Tardy
    Laboratoire d Endocrinologie Mol├ęculaire et Maladies Rares, Centre de Biologie et de Pathologie Est, 69677 Bron Cedex, France
    J Clin Endocrinol Metab 95:1288-300. 2010

Collaborators

Detail Information

Publications8

  1. ncbi request reprint Gene symbol: CYP21A2. Disease: steroid 21-hydroxylase deficiency
    Veronique Tardy
    Laboratoire de Biologie Moleculaire, Hopital Debrousse, Lyon, France
    Hum Genet 119:363. 2006
  2. ncbi request reprint Gene symbol: CYP21A2
    Veronique T V Tardy
    Laboratoire de Biologie Moleculaire, Hopital Debrousse, 29 rue Soeur Bouvier, Lyon Cedex, France
    Hum Genet 121:293. 2007
  3. ncbi request reprint Gene symbol: CYP21A2
    Veronique T V Tardy
    Laboratoire de Biologie Moleculaire, Hopital Debrousse, 29 rue Soeur Bouvier, Lyon Cedex, France
    Hum Genet 121:292. 2007
  4. ncbi request reprint Gene symbol: CYP21A2
    Veronique T V Tardy
    Laboratoire de Biologie Moleculaire, Hopital Debrousse, 29 rue Soeur Bouvier, Lyon Cedex, France
    Hum Genet 121:292-3. 2007
  5. ncbi request reprint Gene symbol: CYP21A2
    Veronique T V Tardy
    Laboratoire de Biologie Moleculaire, Hopital Debrousse, 29 rue Soeur Bouvier, Lyon Cedex, France
    Hum Genet 121:293. 2007
  6. ncbi request reprint Gene symbol: CYP21A2
    Veronique T V Tardy
    Hopital Debrousse, Laboratoire de Biologie Moleculaire, 29 rue Soeur Bouvier, Lyon Cedex, France
    Hum Genet 121:293-4. 2007
  7. ncbi request reprint Gene symbol: CYP21A2
    Veronique T V Tardy
    Hopital Debrousse, Laboratoire de Biologie Moleculaire, 29 rue Soeur Bouvier, Lyon Cedex, France
    Hum Genet 121:294. 2007
  8. doi request reprint Phenotype-genotype correlations of 13 rare CYP21A2 mutations detected in 46 patients affected with 21-hydroxylase deficiency and in one carrier
    V Tardy
    Laboratoire d Endocrinologie Mol├ęculaire et Maladies Rares, Centre de Biologie et de Pathologie Est, 69677 Bron Cedex, France
    J Clin Endocrinol Metab 95:1288-300. 2010
    ..R369W and p.I230T, may be responsible for a severe phenotype underlying the necessity to manage children having them. The p.I230T is a nonclassical mutation, and for the p.R369W, we need more cases to precise its severity...