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Localization of deletion to a 300 Kb interval of chromosome 11q13 in cervical cancer

โœ Scribed by Srivatsan, Eri S; Chakrabarti, Rita; Zainabadi, Kayvan; Pack, Svetlana D; Benyamini, Payam; Mendonca, Marc S; Yang, Pok Kwan; Kang, Kevin; Motamedi, Daria; Sawicki, Mark P


Book ID
110066864
Publisher
Nature Publishing Group
Year
2002
Tongue
English
Weight
868 KB
Volume
21
Category
Article
ISSN
0950-9232

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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