Type 2 diabetes: Evidence for linkage on chromosome 20 in 716 Finnish affected sib pairs

Proceedings of the National Academy of Sciences of the United States of America

Volumn 96, Issue 5, 1999, Pages 2198-2203

  Ghosh, Soumitra ^a   Watanabe, Richard M ^b   Hauser, Elizabeth R ^c   Valle, Timo ^d   Magnuson, Victoria L ^a   Erdos, Michael R ^a   Langefeld, Carl D ^b   Balow Jr , James ^a   Ally, Delphine S ^a   Kohtamaki, Kimmo ^d   Chines, Peter ^a   Birznieks, Gunther ^a   Kaleta, Hong Shi ^b   Musick, Anjene ^a   Te, Catherine ^a   Tannenbaum, Joyce ^a   Eldridge, William ^a   Shapiro, Shane ^a   Martin, Colin ^a   Witt, Alyson ^a   So, Alistair ^a   Chang, Jennie ^a   Shurtleff, Ben ^a   Porter, Rachel ^a   Kudelko, Kristina ^a   Unni, Arun ^a   Segal, Leonid ^a   Sharaf, Ravi ^a   Blaschak Harvan, Jillian ^b   Eriksson, Johan ^d   Tenkula, Tuula ^d   Vidgren, Gabriele ^d   Ehnholm, Christian ^d   Tuomilehto Wolf, Eva ^d   Hagopian, William ^e   Buchanan, Thomas A ^f   Toomilehto, Jaakko ^d   Bergman, Richard N ^g   Collins, Francis S ^a   Boehnke, Michael ^b   more..

^a NATIONAL HUMAN GENOME RESEARCH INSTITUTE   (United States)

^b UNIVERSITY OF MICHIGAN   (United States)

^c DUKE UNIVERSITY MEDICAL CENTER   (United States)

^d NATIONAL PUBLIC HEALTH INSTITUTE   (Finland)

^e UNIVERSITY OF WASHINGTON   (United States)

^f UNIVERSITY OF SOUTHERN CALIFORNIA   (United States)

^g UNIVERSITY OF SOUTHERN CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

NUCLEAR FACTOR;

ADULT; ARTICLE; CHROMOSOME 20; CONTROLLED STUDY; FINLAND; GENETIC LINKAGE; GENETIC SUSCEPTIBILITY; HUMAN; MAJOR CLINICAL STUDY; MATURITY ONSET DIABETES MELLITUS; NON INSULIN DEPENDENT DIABETES MELLITUS; PRIORITY JOURNAL; QUANTITATIVE TRAIT; RECURRENCE RISK; SIBLING; SINGLE STRAND CONFORMATION POLYMORPHISM;

ADULT; BASIC HELIX-LOOP-HELIX LEUCINE ZIPPER TRANSCRIPTION FACTORS; BLOOD GLUCOSE; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 20; DIABETES MELLITUS, TYPE 2; DNA-BINDING PROTEINS; EXONS; FEMALE; FINLAND; GENETIC MARKERS; GENETIC PREDISPOSITION TO DISEASE; GLUCOSE TOLERANCE TEST; HEPATOCYTE NUCLEAR FACTOR 4; HUMANS; INTRONS; LINKAGE (GENETICS); MALE; MIDDLE AGED; MODELS, GENETIC; NUCLEAR FAMILY; ODDS RATIO; PHOSPHOPROTEINS; POINT MUTATION; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; SEQUENCE DELETION; SPOUSES; TRANSCRIPTION FACTORS; VARIATION (GENETICS);

EID: 13044277561     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.96.5.2198     Document Type: Article

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