Differential loss of heterozygosity in familial, sporadic, and uremic hyperparathyroidism

Human Genetics

Volumn 99, Issue 3, 1997, Pages 342-349

  Farnebo, Filip ^a   Teh, Bin Tean ^a   Dotzenrath, Cornelia ^b   Wassif, Wassif S ^c   Svensson, Ann ^a   White, Irene ^a   Betz, Regina ^a   Goretzki, Peter ^b   Sandelin, Kerstin ^a   Farnebo, Lars Ove ^a   Larsson, Catharina ^a  

^a KAROLINSKA UNIVERSITY HOSPITAL   (Sweden)

^b HEINRICH HEINE UNIVERSITY   (Germany)

^c KING'S COLLEGE LONDON   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

CALCIUM;

ARTICLE; CHROMOSOMAL LOCALIZATION; CHROMOSOME 1; CHROMOSOME 11Q; CHROMOSOME 13Q; CHROMOSOME 15Q; CHROMOSOME 2Q; CHROMOSOME 3Q; CHROMOSOME 6Q; FAMILY HISTORY; FLUORESCENCE IN SITU HYBRIDIZATION; GENE LOCUS; GENE MAPPING; HETEROZYGOSITY LOSS; HUMAN; HUMAN TISSUE; HYBRID CELL; HYPERPARATHYROIDISM; MAJOR CLINICAL STUDY; METAPHASE; MULTIPLE ENDOCRINE NEOPLASIA; PARATHYROID ADENOMA; PARATHYROID TUMOR; PRIORITY JOURNAL; TUMOR SUPPRESSOR GENE; X CHROMOSOME;

ADENOMA; AUTORADIOGRAPHY; CALCIUM-BINDING PROTEINS; CHROMOSOME DELETION; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 2; FEMALE; HETEROZYGOTE; HUMANS; HYBRID CELLS; HYPERPARATHYROIDISM; HYPERPARATHYROIDISM, SECONDARY; IN SITU HYBRIDIZATION, FLUORESCENCE; MALE; MULTIPLE ENDOCRINE NEOPLASIA TYPE 1; NEOPLASMS; PARATHYROID NEOPLASMS; RECEPTORS, LDL; UREMIA;

EID: 0031045242     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004390050369     Document Type: Article

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