Localization of the MEN1 gene to a small region within chromosome 11q13 by deletion mapping in tumors (original) (raw)
Alterations of the MEN1 Gene in Sporadic Parathyroid Tumors 1
K. Sandelin
The Journal of Clinical Endocrinology & Metabolism, 1998
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A Family with Isolated Hyperparathyroidism Segregating a Missense MEN1 Mutation and Showing Loss of the Wild-Type Alleles in the Parathyroid Tumors
Bin Teh
The American Journal of Human Genetics, 1998
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Takahiro Okamoto
Surgery, 2000
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Allelic Loss in Parathyroid Tumors from Individuals Homozygous for Multiple Endocrine Neoplasia Type 1 1
Sergio Ortolani
The Journal of Clinical Endocrinology & Metabolism, 1997
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Carcinoma of Two Parathyroid Glands Caused by a Novel MEN1 Gene Mutation – a Rare Feature of the MEN 1 Syndrome
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Medicina, 2011
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Novel association of MEN1 gene mutations with parathyroid carcinoma
Massimiliano Chetta
Oncology letters, 2017
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Germline mutations of the MEN1 gene in familial multiple endocrine neoplasia type 1 and related states
Stephen Marx
Human Molecular Genetics, 1997
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Mutation Analysis of the MEN1 Gene in Multiple Endocrine Neoplasia Type 1, Familial Acromegaly and Familial Isolated Hyperparathyroidism 1
Magnus Nordenskjöld
The Journal of Clinical Endocrinology & Metabolism, 1998
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Germline mutations of the MEN1 gene in familial multiple endocrine neoplasia type …
Lance Liotta
Human Molecular …, 1997
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JT Stewart
2010
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Svetlana Lagercrantz
European Journal of Endocrinology, 2001
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Identification of somatic mutations of the MEN1 gene in sporadic endocrine tumours
Jane Palmer
British journal of …, 2000
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Fine-scale mapping of the gene responsible for multiple endocrine neoplasia type 1 (MEN 1)
Jennifer N . IGWELA
American journal of human genetics, 1992
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Michel Pugeat
Human Molecular Genetics, 1997
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Novel 14 Base-Pair Deletion of the MEN1 Gene in a Patient with Recurrent Primary Hyperparathyroidism
Shinya Uchino
Japanese Journal of Clinical Oncology, 2006
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Localization of the multiple endocrine neoplasia type I (MEN1) gene based on tumor loss of heterozygosity analysis
Lance Liotta
Cancer research, 1997
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Absence of Germ-Line Mutations of the Multiple Endocrine Neoplasia Type 1 ( MEN1 ) Gene in Familial Pituitary Adenoma in Contrast to MEN1 in Japanese 1
Hiroshi Nishioka
The Journal of Clinical Endocrinology & Metabolism, 1998
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Allelic Loss from Chromosome 11 in Parathyroid Tumors
Stephen Marx
1992
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Coincidence of Multiple Endocrine Neoplasia Types 1 and 2: Mutations in theRETProtooncogene andMEN1Tumor Suppressor Gene in a Family Presenting with Recurrent Primary Hyperparathyroidism
Friedhelm Raue
The Journal of Clinical Endocrinology and Metabolism, 2005
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A new mutation of the MEN1 gene in an italian kindred with multiple endocrine neoplasia type 1
Filomena Cetani
European Journal of Endocrinology, 1999
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MEN1 intragenic deletions may represent the most prevalent somatic event in sporadic primary hyperparathyroidism
Paula Soares
European Journal of Endocrinology, 2012
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Multiple endocrine neoplasia type 1 (MEN1) germline mutations in familial isolated primary hyperparathyroidism
Frances A Flinter
Clinical Endocrinology, 2003
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MEN1 gene mutations in Hungarian patients with multiple endocrine neoplasia type 1
Miklós Tóth, Attila Patócs
Clinical Endocrinology, 2007
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Clonal Analysis by Chromosome 11 Microsatellite-PCR of Microdissected Parathyroid Tumors from MEN 1 Patients
Annamaria Morelli
Biochemical and Biophysical Research Communications, 1996
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Localisation of a gene causing endocrine neoplasia to a 4 cM region on chromosome 1p35-p36
John Monson
Journal of Medical Genetics, 1997
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