Identification of susceptibility genes for complex metabolic diseases

Annals of the New York Academy of Sciences

Volumn 967, Issue , 2002, Pages 1-6

  Bogardus, Clifton ^a   Baier, Leslie ^a   Permana, Paska ^a   Prochazka, Michal ^a   Wolford, Johanna ^a   Hanson, Robert ^a  

^a NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES   (United States)

Author keywords

Allele; Genetic; Linkage; Mendelian non Mendelian disease; Positional cloning; Subphenotype; Susceptibility genes

Indexed keywords

DNA;

CONFERENCE PAPER; DIABETES MELLITUS; EXPRESSED SEQUENCE TAG; GENE IDENTIFICATION; GENETIC DISORDER; GENETIC LINKAGE; GENETIC MARKER; GENETIC SUSCEPTIBILITY; HUMAN; HYPERLIPIDEMIA; HYPERTENSION; METABOLIC DISORDER; MOLECULAR CLONING; PHENOTYPE; SEGREGATION ANALYSIS; SINGLE NUCLEOTIDE POLYMORPHISM; SYNDROME X;

EID: 0036294712     PISSN: 00778923     EISSN: None     Source Type: Book Series    
DOI: 10.1111/j.1749-6632.2002.tb04257.x     Document Type: Conference Paper

References (8)

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7. Mutations in the hepatocyte nuclear factor-1 alpha gene in maturity-onset diabetes of the young (MODY3)
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