Growth Hormone Insensitivity (Laron Syndrome) in a Russian Girl of Slavic Origin Caused by a Common Mutation of the GH Receptor Gene

A.N. Tiulpakov,; I.V. Orlovsky,; N.U. Kalintchenko,; D.A. Lonina,; G.S. Kalesnikova,; V.A. Peterkova,; R. Bjamason,; L. Baumbach,; P.M. Rubtsov,

doi:10.1515/IJDHD.1999.1.2.95

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Growth Hormone Insensitivity (Laron Syndrome) in a Russian Girl of Slavic Origin Caused by a Common Mutation of the GH Receptor Gene

A.N. Tiulpakov, , I.V. Orlovsky, , N.U. Kalintchenko, , D.A. Lonina, , G.S. Kalesnikova, , V.A. Peterkova, , R. Bjamason, , L. Baumbach, and P.M. Rubtsov,

Published/Copyright: April 1, 1999

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

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Tiulpakov,, A.N., Orlovsky,, I.V., Kalintchenko,, N.U., Lonina,, D.A., Kalesnikova,, G.S., Peterkova,, V.A., Bjamason,, R., Baumbach,, L. and Rubtsov,, P.M.. "Growth Hormone Insensitivity (Laron Syndrome) in a Russian Girl of Slavic Origin Caused by a Common Mutation of the GH Receptor Gene" International Journal on Disability and Human Development, vol. 1, no. 2, pp. 95-100. https://doi.org/10.1515/IJDHD.1999.1.2.95

Tiulpakov,, A., Orlovsky,, I., Kalintchenko,, N., Lonina,, D., Kalesnikova,, G., Peterkova,, V., Bjamason,, R., Baumbach,, L. & Rubtsov,, P. (). Growth Hormone Insensitivity (Laron Syndrome) in a Russian Girl of Slavic Origin Caused by a Common Mutation of the GH Receptor Gene. International Journal on Disability and Human Development, 1(2), 95-100. https://doi.org/10.1515/IJDHD.1999.1.2.95

Tiulpakov,, A., Orlovsky,, I., Kalintchenko,, N., Lonina,, D., Kalesnikova,, G., Peterkova,, V., Bjamason,, R., Baumbach,, L. and Rubtsov,, P. () Growth Hormone Insensitivity (Laron Syndrome) in a Russian Girl of Slavic Origin Caused by a Common Mutation of the GH Receptor Gene. International Journal on Disability and Human Development, Vol. 1 (Issue 2), pp. 95-100. https://doi.org/10.1515/IJDHD.1999.1.2.95

Tiulpakov,, A.N., Orlovsky,, I.V., Kalintchenko,, N.U., Lonina,, D.A., Kalesnikova,, G.S., Peterkova,, V.A., Bjamason,, R., Baumbach,, L. and Rubtsov,, P.M.. "Growth Hormone Insensitivity (Laron Syndrome) in a Russian Girl of Slavic Origin Caused by a Common Mutation of the GH Receptor Gene" International Journal on Disability and Human Development 1, no. 2 (): 95-100. https://doi.org/10.1515/IJDHD.1999.1.2.95

Tiulpakov, A, Orlovsky, I, Kalintchenko, N, Lonina, D, Kalesnikova, G, Peterkova, V, Bjamason, R, Baumbach, L, Rubtsov, P. Growth Hormone Insensitivity (Laron Syndrome) in a Russian Girl of Slavic Origin Caused by a Common Mutation of the GH Receptor Gene. International Journal on Disability and Human Development. ;1(2): 95-100. https://doi.org/10.1515/IJDHD.1999.1.2.95

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https://doi.org/10.1515/IJDHD.1999.1.2.95

Articles in the same Issue

CONTENTS
Letter from the Editors
Glucocorticoid Receptor Isoforms Alpha and Beta: Potential Physiological and Pathological Importance
NeuroD/Beta2 Polymorphism is Not Associated with Type 1 Diabetes in Chinese, Korean, or Caucasian Populations
CYP11B1 Intragenic Polymorphisms Give Evidence for a Different Q356X Allele in an African-Brazilian Patient
Mutations in the CFTR Gene are Not a Common Finding in Patients with Diabetes
A Novel Mutation (W718S) in the Steroid-Binding Domain of the Androgen Receptor Gene in a Boy with Ambiguous Genitalia and Hypergonadotrophic Hypogonadism
Growth Hormone Insensitivity (Laron Syndrome) in a Russian Girl of Slavic Origin Caused by a Common Mutation of the GH Receptor Gene
Homozygous Transthyretin Leu64: A Very Rare Transthyretin Mutation Associated With Amyloidosis but Not With Euthyroid Hyperthyroxinemia
FORUM AND CORRESPONDENCE. BOOK REVIEWS. CALENDAR