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Clinical, Hormonal and Molecular Genetic Characterization of Hungarian Patients with 11β-Hydroxylase Deficiency

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Published/Copyright: January 1, 2001
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International Journal on Disability and Human Development
From the journal International Journal on Disability and Human Development Volume 2 Issue 1

Published Online: 2001-01

©2011 by Walter de Gruyter GmbH & Co.

Articles in the same Issue

  1. CONTENTS
  2. Letter from the Editors
  3. Molecular Genetics of Familial Hyperparathyroidism
  4. Mutational Analysis of the Estrogen Receptor Alpha Gene in Israeli Osteoporotic Men and Women
  5. Somatic Mutation Analysis of the MEN1 Gene in Adrenocortical Tumors Using Denaturing Gradient Gel Electrophoresis (DGGE)
  6. The Human Germ Cell-Less (HGCL): A Candidate Gene for Alström Syndrome
  7. Clinical, Hormonal and Molecular Genetic Characterization of Hungarian Patients with 11β-Hydroxylase Deficiency
  8. Molecular Analysis of the Growth Hormone Gene (GH1) in Isolated Growth Hormone Deficiency
  9. A Novel Polymorphism in Exon 4 of the Growth Hormone Gene and Association of Short Stature with a Known 5' UTR Polymorphism
  10. Complete Deficiency of Growth Hormone, Thyrotropin and Prolactin in Two Siblings: A New Pit-1 Mutation
  11. BOOK REVIEWS. CALENDAR
https://doi.org/10.1515/IJDHD.2001.2.1.37

Articles in the same Issue

  1. CONTENTS
  2. Letter from the Editors
  3. Molecular Genetics of Familial Hyperparathyroidism
  4. Mutational Analysis of the Estrogen Receptor Alpha Gene in Israeli Osteoporotic Men and Women
  5. Somatic Mutation Analysis of the MEN1 Gene in Adrenocortical Tumors Using Denaturing Gradient Gel Electrophoresis (DGGE)
  6. The Human Germ Cell-Less (HGCL): A Candidate Gene for Alström Syndrome
  7. Clinical, Hormonal and Molecular Genetic Characterization of Hungarian Patients with 11β-Hydroxylase Deficiency
  8. Molecular Analysis of the Growth Hormone Gene (GH1) in Isolated Growth Hormone Deficiency
  9. A Novel Polymorphism in Exon 4 of the Growth Hormone Gene and Association of Short Stature with a Known 5' UTR Polymorphism
  10. Complete Deficiency of Growth Hormone, Thyrotropin and Prolactin in Two Siblings: A New Pit-1 Mutation
  11. BOOK REVIEWS. CALENDAR
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