Molecular Genetics of Familial Hyperparathyroidism

A. Villablanca,; A. Höög,; C. Larsson,; B.T. Teh,

doi:10.1515/IJDHD.2001.2.1.3

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Molecular Genetics of Familial Hyperparathyroidism

A. Villablanca, , A. Höög, , C. Larsson, and B.T. Teh,

Published/Copyright: January 1, 2001

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From the journal International Journal on Disability and Human Development Volume 2 Issue 1

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Harvard
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Villablanca,, A., Höög,, A., Larsson,, C. and Teh,, B.T.. "Molecular Genetics of Familial Hyperparathyroidism" International Journal on Disability and Human Development, vol. 2, no. 1, 2001, pp. 3-12. https://doi.org/10.1515/IJDHD.2001.2.1.3

Villablanca,, A., Höög,, A., Larsson,, C. & Teh,, B. (2001). Molecular Genetics of Familial Hyperparathyroidism. International Journal on Disability and Human Development, 2(1), 3-12. https://doi.org/10.1515/IJDHD.2001.2.1.3

Villablanca,, A., Höög,, A., Larsson,, C. and Teh,, B. (2001) Molecular Genetics of Familial Hyperparathyroidism. International Journal on Disability and Human Development, Vol. 2 (Issue 1), pp. 3-12. https://doi.org/10.1515/IJDHD.2001.2.1.3

Villablanca,, A., Höög,, A., Larsson,, C. and Teh,, B.T.. "Molecular Genetics of Familial Hyperparathyroidism" International Journal on Disability and Human Development 2, no. 1 (2001): 3-12. https://doi.org/10.1515/IJDHD.2001.2.1.3

Villablanca, A, Höög, A, Larsson, C, Teh, B. Molecular Genetics of Familial Hyperparathyroidism. International Journal on Disability and Human Development. 2001;2(1): 3-12. https://doi.org/10.1515/IJDHD.2001.2.1.3

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

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https://doi.org/10.1515/IJDHD.2001.2.1.3

Articles in the same Issue

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