Exclusion of candidate genes in two families with autosomal dominant hypocalcified amelogenesis imperfecta

European Journal of Oral Sciences

Volumn 111, Issue 4, 2003, Pages 326-331

  Hart, P Suzanne ^a   Wright, J Timothy ^b   Savage, Mathew ^b   Kang, George ^b   Bensen, Jeannette T ^c   Gorry, Michael C ^d   Hart, Thomas C ^d  

^a UNIVERSITY OF PITTSBURGH GRADUATE SCHOOL OF PUBLIC HEALTH   (United States)

^b UNIVERSITY OF NORTH CAROLINA   (United States)

^c WAKE FOREST BAPTIST HEALTH   (United States)

^d UNIVERSITY OF PITTSBURGH   (United States)

Author keywords

Ameloblastin; Enamel; Enamelin; Enamelysin; Kallikrein 4; Tuftelin

Indexed keywords

KALLIKREIN; SCLEROPROTEIN; AMBN PROTEIN, HUMAN; DNA; ENAMEL PROTEIN; KALLIKREIN 4; MATRIX METALLOPROTEINASE; MATRIX METALLOPROTEINASE 20; MMP20 PROTEIN, HUMAN; TUFTELIN;

AMELOBLAST; AMELOGENESIS IMPERFECTA; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CHROMOSOME 11Q; CHROMOSOME 19Q; CHROMOSOME 1Q; CHROMOSOME 4Q; DISEASE MARKER; ENAMEL HYPOPLASIA; GENE EXPRESSION; GENE IDENTIFICATION; GENE LOCATION; GENE MUTATION; GENETIC HETEROGENEITY; GENETIC LINKAGE; GENETIC TRAIT; GENETIC VARIABILITY; HUMAN; CHROMOSOME 1; CHROMOSOME 11; CHROMOSOME 19; CHROMOSOME 4; CHROMOSOME MAP; DOMINANT GENE; FEMALE; GENETIC MARKER; GENETICS; MALE; MUTATION; TOOTH DEVELOPMENT;

AMELOGENESIS IMPERFECTA; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 1; CHROMOSOMES, HUMAN, PAIR 11; CHROMOSOMES, HUMAN, PAIR 19; CHROMOSOMES, HUMAN, PAIR 4; DENTAL ENAMEL PROTEINS; DNA; FEMALE; GENES, DOMINANT; GENETIC MARKERS; HUMANS; KALLIKREINS; LINKAGE (GENETICS); LOD SCORE; MALE; MATRIX METALLOPROTEINASE 20; MATRIX METALLOPROTEINASES; MUTATION; TOOTH CALCIFICATION;

EID: 0141497179     PISSN: 09098836     EISSN: None     Source Type: Journal    
DOI: 10.1034/j.1600-0722.2003.00046.x     Document Type: Article

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