Haplosufficiency of the melanocortin-4 receptor gene in individuals with deletions of 18q

Human Genetics

Volumn 105, Issue 5, 1999, Pages 424-427

  Cody, J D ^a   Reveles, X T ^a   Hale, D E ^a   Lehman, D ^a   Coon, H ^a   Leach, R J ^a  

^a UNIVERSITY OF TEXAS HEALTH SCIENCE CENTER AT SAN ANTONIO   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

MELANOCORTIN RECEPTOR; MELANOCORTIN 4 RECEPTOR; PRIMER DNA; RECEPTOR;

ARTICLE; CHROMOSOME 18Q; CLINICAL ARTICLE; DISEASE SEVERITY; GENE DELETION; HEMIZYGOSITY; HUMAN; HUMAN CELL; OBESITY; PRIORITY JOURNAL; RECEPTOR GENE; BIOLOGICAL MODEL; CHROMOSOME 18; CHROMOSOME DELETION; DOMINANT GENE; GENETICS; HAPLOTYPE; NUCLEOTIDE SEQUENCE; PATHOLOGY; PHENOTYPE;

BASE SEQUENCE; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 18; DNA PRIMERS; GENES, DOMINANT; HAPLOTYPES; HUMANS; MODELS, GENETIC; OBESITY; PHENOTYPE; RECEPTOR, MELANOCORTIN, TYPE 4; RECEPTORS, PEPTIDE;

EID: 0032585961     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004390051125     Document Type: Article

References (12)