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An Infrequent Double Mutation in the MEN1 Gene
-
G. Pérez de Nanclares,
Veröffentlicht/Copyright:
1. Oktober 2001
Published Online: 2001-10
©2011 by Walter de Gruyter GmbH & Co.
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Artikel in diesem Heft
- CONTENTS
- Letter from the Editors
- Molecular Genetics of Thyroid Disorders in the Neonate: A Review
- Molecular Analysis of the Growth Hormone Releasing Hormone Receptor (GHRH-R) Gene in Isolated Growth Hormone Deficiency: Identification of a Likely Etiological Mutation in the Signal Peptide
- Adrenal Mass in Carney Triad
- An Infrequent Double Mutation in the MEN1 Gene
- X-linked Adrenoleukodystrophy: Unusual Clinical Manifestation
- BOOK REVIEWS. CALENDAR. INDEX
Artikel in diesem Heft
- CONTENTS
- Letter from the Editors
- Molecular Genetics of Thyroid Disorders in the Neonate: A Review
- Molecular Analysis of the Growth Hormone Releasing Hormone Receptor (GHRH-R) Gene in Isolated Growth Hormone Deficiency: Identification of a Likely Etiological Mutation in the Signal Peptide
- Adrenal Mass in Carney Triad
- An Infrequent Double Mutation in the MEN1 Gene
- X-linked Adrenoleukodystrophy: Unusual Clinical Manifestation
- BOOK REVIEWS. CALENDAR. INDEX
