Multiple endocrine neoplasia type 1 syndrome (MEN1, MIM 131100), an autosomal dominant disease, is characterized by parathyroid hyperplasia, pancreatic endocrine tumors, and pituitary adenomas. These tumors also occur sporadically. Both the familial (MEN1) and the sporadic tumors reveal loss of hete
✦ LIBER ✦
Localization of Multiple Melanoma Tumor–Suppressor Genes on Chromosome 11 by Use of Homozygosity Mapping-of-Deletions Analysis
✍ Scribed by Eleonora K. Goldberg; J. Michael Glendening; Zarir Karanjawala; Anjali Sridhar; Graeme J. Walker; Nicholas K. Hayward; Andrew J. Rice; Devinda Kurera; Yasmine Tebha; Jane W. Fountain
- Book ID
- 117853369
- Publisher
- American Society of Human Genetics
- Year
- 2000
- Tongue
- English
- Weight
- 833 KB
- Volume
- 67
- Category
- Article
- ISSN
- 0002-9297
- DOI
- 10.1086/302999
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