Familial Isolated Primary Hyperparathyroidism in a Large Georgian-Jewish Kindred: Genetic Studies

D. Olchovsky,; M.R. Hobbs,; E. Pras,; I. Shimon,; J. Silver,; L. Irmin,; E. Friedman,

doi:10.1515/IJDHD.2001.2.2.91

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

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Olchovsky,, D., Hobbs,, M.R., Pras,, E., Shimon,, I., Silver,, J., Irmin,, L. and Friedman,, E.. "Familial Isolated Primary Hyperparathyroidism in a Large Georgian-Jewish Kindred: Genetic Studies" International Journal on Disability and Human Development, vol. 2, no. 2, pp. 91-98. https://doi.org/10.1515/IJDHD.2001.2.2.91

Olchovsky,, D., Hobbs,, M., Pras,, E., Shimon,, I., Silver,, J., Irmin,, L. & Friedman,, E. (). Familial Isolated Primary Hyperparathyroidism in a Large Georgian-Jewish Kindred: Genetic Studies. International Journal on Disability and Human Development, 2(2), 91-98. https://doi.org/10.1515/IJDHD.2001.2.2.91

Olchovsky,, D., Hobbs,, M., Pras,, E., Shimon,, I., Silver,, J., Irmin,, L. and Friedman,, E. () Familial Isolated Primary Hyperparathyroidism in a Large Georgian-Jewish Kindred: Genetic Studies. International Journal on Disability and Human Development, Vol. 2 (Issue 2), pp. 91-98. https://doi.org/10.1515/IJDHD.2001.2.2.91

Olchovsky,, D., Hobbs,, M.R., Pras,, E., Shimon,, I., Silver,, J., Irmin,, L. and Friedman,, E.. "Familial Isolated Primary Hyperparathyroidism in a Large Georgian-Jewish Kindred: Genetic Studies" International Journal on Disability and Human Development 2, no. 2 (): 91-98. https://doi.org/10.1515/IJDHD.2001.2.2.91

Olchovsky, D, Hobbs, M, Pras, E, Shimon, I, Silver, J, Irmin, L, Friedman, E. Familial Isolated Primary Hyperparathyroidism in a Large Georgian-Jewish Kindred: Genetic Studies. International Journal on Disability and Human Development. ;2(2): 91-98. https://doi.org/10.1515/IJDHD.2001.2.2.91

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CONTENTS
Letter from the Editors
Neonatal Hemochromatosis - Immunological, Metabolic or Genetic?
Molecular, Cytogenetic, Hormonal and Clinical Characterization of Ten XX Males Including Genetic Counseling
Familial Isolated Primary Hyperparathyroidism in a Large Georgian-Jewish Kindred: Genetic Studies
A Novel Frameshift Mutation of the DAX-1 Gene in a Boy with X-Linked Adrenal Hypoplasia Congenita and No Early Impairment of the Hypothalamus-Pituitary-Gonadal Axis
A Novel AVP-Neurophysin Gene Mutation in Familial Neurohypophyseal Diabetes Insipidus Presenting with Nocturnal Enuresis
Detection of AIRE Mutation in Atypical Autoimmune Polyglandular Syndrome Type 1 (APS1)
BOOK REVIEWS. CALENDAR

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https://doi.org/10.1515/IJDHD.2001.2.2.91

Articles in the same Issue

CONTENTS
Letter from the Editors
Neonatal Hemochromatosis - Immunological, Metabolic or Genetic?
Molecular, Cytogenetic, Hormonal and Clinical Characterization of Ten XX Males Including Genetic Counseling
Familial Isolated Primary Hyperparathyroidism in a Large Georgian-Jewish Kindred: Genetic Studies
A Novel Frameshift Mutation of the DAX-1 Gene in a Boy with X-Linked Adrenal Hypoplasia Congenita and No Early Impairment of the Hypothalamus-Pituitary-Gonadal Axis
A Novel AVP-Neurophysin Gene Mutation in Familial Neurohypophyseal Diabetes Insipidus Presenting with Nocturnal Enuresis
Detection of AIRE Mutation in Atypical Autoimmune Polyglandular Syndrome Type 1 (APS1)
BOOK REVIEWS. CALENDAR