Mutations in the CFTR Gene are Not a Common Finding in Patients with Diabetes

R. Gill-Randall,; L. Evans,; J.C. Alcolado,

doi:10.1515/IJDHD.1999.1.2.87

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Mutations in the CFTR Gene are Not a Common Finding in Patients with Diabetes

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

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Gill-Randall,, R., Evans,, L. and Alcolado,, J.C.. "Mutations in the CFTR Gene are Not a Common Finding in Patients with Diabetes" International Journal on Disability and Human Development, vol. 1, no. 2, pp. 87-90. https://doi.org/10.1515/IJDHD.1999.1.2.87

Gill-Randall,, R., Evans,, L. & Alcolado,, J. (). Mutations in the CFTR Gene are Not a Common Finding in Patients with Diabetes. International Journal on Disability and Human Development, 1(2), 87-90. https://doi.org/10.1515/IJDHD.1999.1.2.87

Gill-Randall,, R., Evans,, L. and Alcolado,, J. () Mutations in the CFTR Gene are Not a Common Finding in Patients with Diabetes. International Journal on Disability and Human Development, Vol. 1 (Issue 2), pp. 87-90. https://doi.org/10.1515/IJDHD.1999.1.2.87

Gill-Randall,, R., Evans,, L. and Alcolado,, J.C.. "Mutations in the CFTR Gene are Not a Common Finding in Patients with Diabetes" International Journal on Disability and Human Development 1, no. 2 (): 87-90. https://doi.org/10.1515/IJDHD.1999.1.2.87

Gill-Randall, R, Evans, L, Alcolado, J. Mutations in the CFTR Gene are Not a Common Finding in Patients with Diabetes. International Journal on Disability and Human Development. ;1(2): 87-90. https://doi.org/10.1515/IJDHD.1999.1.2.87

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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

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https://doi.org/10.1515/IJDHD.1999.1.2.87

Artikel in diesem Heft

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