The Parathyroid/Pituitary Variant of Multiple Endocrine Neoplasia Type 1 Usually Has Causes Other thanp27Kip1Mutations

Author:

Ozawa Atsushi1,Agarwal Sunita K.1,Mateo Carmen M.1,Burns A. Lee1,Rice Terri S.1,Kennedy Patricia A.1,Quigley Caitlin M.1,Simonds William F.1,Weinstein Lee S.1,Chandrasekharappa Settara C.2,Collins Francis S.2,Spiegel Allen M.1,Marx Stephen J.1

Affiliation:

1. Metabolic Diseases Branch (A.O., S.K.A., C.M.M., A.L.B., T.S.R., P.A.K., C.M.Q., W.F.S., L.S.W., A.M.S., S.J.M.), National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health (NIH), Bethesda, Maryland 20892

2. Genome Technology Branch (S.C.C., F.S.C.), National Human Genome Research Institute, NIH, Bethesda, Maryland 20892

Publisher

The Endocrine Society

Subject

Biochemistry (medical),Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference20 articles.

1. Guidelines for diagnosis and therapy of MEN type 1 and type 2.;Brandi;J Clin Endocrinol Metab,2001

2. Multiple endocrine neoplasia type 1;Marx;In: Vogelstein B, Kinzler KW, eds. The genetic basis of human cancer. 2nd ed. New York: McGraw Hill;,2002

3. Familial isolated hyperparathyroidism: clinical and genetic characteristics of thirty-six kindreds.;Simonds;Medicine,2002

4. Clinical characterization of familial isolated pituitary adenomas.;Daly;J Clin Endocrinol Metab,2006

5. Detection of an MEN1gene mutation depends on clinical features and supports current referral criteria for diagnostic molecular genetic testing.;Ellard;Clin Endocrinol (Oxf),2005

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