HHEX-IDE polymorphism is associated with low birth weight in offspring with a family history of type 1 diabetes

Journal of Clinical Endocrinology and Metabolism

Volumn 94, Issue 10, 2009, Pages 4113-4115

  Winkler, Christiane ^a   Illig, Thomas ^a   Koczwara, Kerstin ^a   Bonifacio, Ezio ^b   Ziegler, Anette Gabriele ^a,c  

^a INSTITUTE OF EPIDEMIOLOGY   (Germany)

^b DRESDEN UNIVERSITY OF TECHNOLOGY   (Germany)

^c TECHNICAL UNIVERSITY OF MUNICH   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

GLYCOSYLATED HEMOGLOBIN;

ALLELE; ARTICLE; CHILD; COHORT ANALYSIS; CORRELATION ANALYSIS; FAMILY HISTORY; FEMALE; GENE LOCUS; GENETIC RISK; GENETIC VARIABILITY; GENOTYPE; GERMANY; HEMOGLOBIN DETERMINATION; HUMAN; INSULIN DEPENDENT DIABETES MELLITUS; LOW BIRTH WEIGHT; MAJOR CLINICAL STUDY; MALE; NON INSULIN DEPENDENT DIABETES MELLITUS; PRIORITY JOURNAL; PROGENY; SINGLE NUCLEOTIDE POLYMORPHISM;

EID: 70349925566     PISSN: 0021972X     EISSN: 0021972X     Source Type: Journal    
DOI: 10.1210/jc.2009-0970     Document Type: Article

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