A genotypic and histopathological study of a large Dutch kindred with hyperparathyroidism-jaw tumor syndrome

Journal of Clinical Endocrinology and Metabolism

Volumn 85, Issue 4, 2000, Pages 1449-1454

  Haven, Carola Jose ^a   Wong, Fung Ki ^b   Van Dam, Eveline W C M ^a   Van Der Luijt, Rob ^a,c   Van Asperen, Christi ^a   Jansen, Joke ^c   Rosenberg, Carla ^a   De Wit, Mireille ^c   Roijers, Janine ^c   Hoppener, Jo ^c   Lips, Cornelis J ^b,c   Larsson, Catharina ^a   Teh, Bin Tean ^d   Morreau, Hans ^a  

^a LEIDEN UNIVERSITY MEDICAL CENTER   (Netherlands)

^b KAROLINSKA UNIVERSITY HOSPITAL   (Sweden)

^c UNIVERSITY MEDICAL CENTER UTRECHT   (Netherlands)

^d Van Andel Research Center   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME 1Q; CLINICAL ARTICLE; ENDOCRINE TUMOR; GENE MUTATION; GENOTYPE; GERM CELL TUMOR; HAMARTOMA; HUMAN; HUMAN TISSUE; JAW TUMOR; KIDNEY ADENOMA; KIDNEY CARCINOMA; KIDNEY CYST; MULTIPLE ENDOCRINE NEOPLASIA; NEPHROBLASTOMA; NETHERLANDS; ONCOCYTOMA; OSSIFYING FIBROMA; PANCREAS ADENOCARCINOMA; PEDIGREE ANALYSIS; PRIMARY HYPERPARATHYROIDISM; PRIORITY JOURNAL; SEMINOMA; THYROID ADENOMA;

CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 1; FEMALE; GENETIC MARKERS; GENOTYPE; HUMANS; HYPERPARATHYROIDISM; JAW NEOPLASMS; LOD SCORE; LOSS OF HETEROZYGOSITY; MALE; MULTIPLE ENDOCRINE NEOPLASIA TYPE 1; MUTATION; NETHERLANDS; PEDIGREE; RECOMBINATION, GENETIC; SYNDROME;

EID: 17744379773     PISSN: 0021972X     EISSN: None     Source Type: Journal    
DOI: 10.1210/jc.85.4.1449     Document Type: Article

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