CYP11B1 Intragenic Polymorphisms Give Evidence for a Different Q356X Allele in an African-Brazilian Patient

C.E. De Carvalho,; J.Y. Penachioni,; M. Castro,; A.C. Moreira,; M.P. De Mello,

doi:10.1515/IJDHD.1999.1.2.79

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CYP11B1 Intragenic Polymorphisms Give Evidence for a Different Q356X Allele in an African-Brazilian Patient

C.E. De Carvalho, , J.Y. Penachioni, , M. Castro, , A.C. Moreira, und M.P. De Mello,

Veröffentlicht/Copyright: 1. April 1999

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

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De Carvalho,, C.E., Penachioni,, J.Y., Castro,, M., Moreira,, A.C. and De Mello,, M.P.. "CYP11B1 Intragenic Polymorphisms Give Evidence for a Different Q356X Allele in an African-Brazilian Patient" International Journal on Disability and Human Development, vol. 1, no. 2, pp. 79-86. https://doi.org/10.1515/IJDHD.1999.1.2.79

De Carvalho,, C., Penachioni,, J., Castro,, M., Moreira,, A. & De Mello,, M. (). CYP11B1 Intragenic Polymorphisms Give Evidence for a Different Q356X Allele in an African-Brazilian Patient. International Journal on Disability and Human Development, 1(2), 79-86. https://doi.org/10.1515/IJDHD.1999.1.2.79

De Carvalho,, C., Penachioni,, J., Castro,, M., Moreira,, A. and De Mello,, M. () CYP11B1 Intragenic Polymorphisms Give Evidence for a Different Q356X Allele in an African-Brazilian Patient. International Journal on Disability and Human Development, Vol. 1 (Issue 2), pp. 79-86. https://doi.org/10.1515/IJDHD.1999.1.2.79

De Carvalho,, C.E., Penachioni,, J.Y., Castro,, M., Moreira,, A.C. and De Mello,, M.P.. "CYP11B1 Intragenic Polymorphisms Give Evidence for a Different Q356X Allele in an African-Brazilian Patient" International Journal on Disability and Human Development 1, no. 2 (): 79-86. https://doi.org/10.1515/IJDHD.1999.1.2.79

De Carvalho, C, Penachioni, J, Castro, M, Moreira, A, De Mello, M. CYP11B1 Intragenic Polymorphisms Give Evidence for a Different Q356X Allele in an African-Brazilian Patient. International Journal on Disability and Human Development. ;1(2): 79-86. https://doi.org/10.1515/IJDHD.1999.1.2.79

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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.1999.1.2.79

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