Letter from the Editors

doi:10.1515/IJDHD.2000.1.3.113

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Letter from the Editors

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Aus der Zeitschrift International Journal on Disability and Human Development Band 1 Heft 3

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"Letter from the Editors" International Journal on Disability and Human Development, vol. 1, no. 3, pp. 113-114. https://doi.org/10.1515/IJDHD.2000.1.3.113

(). Letter from the Editors. International Journal on Disability and Human Development, 1(3), 113-114. https://doi.org/10.1515/IJDHD.2000.1.3.113

() Letter from the Editors. International Journal on Disability and Human Development, Vol. 1 (Issue 3), pp. 113-114. https://doi.org/10.1515/IJDHD.2000.1.3.113

"Letter from the Editors" International Journal on Disability and Human Development 1, no. 3 (): 113-114. https://doi.org/10.1515/IJDHD.2000.1.3.113

Letter from the Editors. International Journal on Disability and Human Development. ;1(3): 113-114. https://doi.org/10.1515/IJDHD.2000.1.3.113

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Published Online: 2000-07

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Artikel in diesem Heft

CONTENTS
Letter from the Editors
Prader-Willi and Angelman Syndromes: Diagnostic Approach
Argl83His, a New Mutational "Hot-Spot" in the Growth Hormone Gene
Novel Mutation (Arg836ter) of the Sulfonylurea Receptor-1 (SUR1) Gene in Congenital Hyperinsulinism
De novo RET Mutation Positive Multiple Endocrine Neoplasia Type 2B and Hereditary Nonpolyposis Colorectal Cancer Syndrome Occurring in the Same Family: Parent-of-Origin and Mismatch Repair
Bromocriptine Resistant Prolactinomas and Non-Functioning Pituitary Tumors: Somatic Mutational Analyses of the Dopamine Type 2 Receptor and the MEN1 Gene
Genetic Studies in Familial Aldosteronism Not Suppressible by Dexamethasone
Recombination Between the Sodium Channel SCN8A and the Allgrove Syndrome Gene in a Puerto Rican Kindred
BOOK REVIEWS. CALENDAR

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https://doi.org/10.1515/IJDHD.2000.1.3.113

Artikel in diesem Heft

CONTENTS
Letter from the Editors
Prader-Willi and Angelman Syndromes: Diagnostic Approach
Argl83His, a New Mutational "Hot-Spot" in the Growth Hormone Gene
Novel Mutation (Arg836ter) of the Sulfonylurea Receptor-1 (SUR1) Gene in Congenital Hyperinsulinism
De novo RET Mutation Positive Multiple Endocrine Neoplasia Type 2B and Hereditary Nonpolyposis Colorectal Cancer Syndrome Occurring in the Same Family: Parent-of-Origin and Mismatch Repair
Bromocriptine Resistant Prolactinomas and Non-Functioning Pituitary Tumors: Somatic Mutational Analyses of the Dopamine Type 2 Receptor and the MEN1 Gene
Genetic Studies in Familial Aldosteronism Not Suppressible by Dexamethasone
Recombination Between the Sodium Channel SCN8A and the Allgrove Syndrome Gene in a Puerto Rican Kindred
BOOK REVIEWS. CALENDAR