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Prader-Willi and Angelman Syndromes: Diagnostic Approach
-
D. Abeliovich,
Published/Copyright:
July 1, 2000
Published Online: 2000-07
©2011 by Walter de Gruyter GmbH & Co.
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Articles in the same Issue
- 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
Articles in the same Issue
- 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
