Jaw lesions and hyperparathyroidism [1]

Journal of Oral and Maxillofacial Surgery

Volumn 62, Issue 4, 2004, Pages 519-

  Aldred, Michael J ^a   Talacko, Anna A ^a   Savarirayan, Ravi ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

CLINICAL FEATURE; DIFFERENTIAL DIAGNOSIS; DISEASE ASSOCIATION; FAMILY HISTORY; FIBROMA; GENETIC COUNSELING; HUMAN; HYPERPARATHYROIDISM; HYPERTHYROIDISM JAW TUMOR SYNDROME; INHERITANCE; JAW DISEASE; LETTER; OSSIFICATION; PARATHYROID CARCINOMA; PHYSICAL EXAMINATION;

EID: 1842425933     PISSN: 02782391     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.joms.2004.01.004     Document Type: Letter

References (3)

1. National Center for Biotechnology Information: Online Mendelian Inheritance in Man, OMIM.™ Johns Hopkins University, Baltimore, MD. MIM Number: 145001: 11/27/2002. Available at: http://www.ncbi.nlm.nih.gov/omim. Accessed January 16, 2004
2. Carpten JD, Robbins CM, Villablanca A, et al: HRPT2, encoding parafibromin, is mutated in hyperparathyroidism-jaw tumor syndrome. Nat Genet 32:676, 2002
3. Pidwimy GN, Szabo J, Hobbs M, et al: Followup of two hyperparathyroidism-jaw tumor syndrome families reported in 1971 and 1981 reveals that they are related and that parathyroid cancer is a part of the syndrome. Am J Hum Genet 57:A75, 1995 (abstr)