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, und B.T. Teh,

Veröffentlicht/Copyright: 1. Januar 2001

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Aus der Zeitschrift International Journal on Disability and Human Development Band 2 Heft 1

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APA
Harvard
Chicago
Vancouver

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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Published Online: 2001-01

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Artikel in diesem Heft

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

Artikel in diesem Heft

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