Genetic associations with neonatal thyroid-stimulating hormone levels

Pediatric Research

Volumn 73, Issue 4, 2013, Pages 484-491

  Alul, Farah Y ^a   Shchelochkov, Oleg A ^a   Berberich, Stanton L ^b   Murray, Jeffrey C ^a   Ryckman, Kelli K ^a  

^a UNIVERSITY OF IOWA   (United States)

^b UNIVERSITY OF IOWA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

THYROTROPIN;

ALLELE; ARTICLE; BIRTH; CHROMOSOME 9; COHORT ANALYSIS; FEMALE; GENETIC ASSOCIATION; GENOTYPE; GESTATIONAL AGE; HAPLOTYPE; HUMAN; MAJOR CLINICAL STUDY; MALE; NEWBORN; PREMATURITY; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; STATISTICAL SIGNIFICANCE; THYROID DISEASE; THYROTROPIN BLOOD LEVEL; TOTAL PARENTERAL NUTRITION; UNITED STATES;

3',5'-CYCLIC-AMP PHOSPHODIESTERASES; ANALYSIS OF VARIANCE; BIOLOGICAL MARKERS; CHI-SQUARE DISTRIBUTION; CHROMOSOMES, HUMAN, PAIR 9; FEMALE; FORKHEAD TRANSCRIPTION FACTORS; GENE FREQUENCY; GENETIC ASSOCIATION STUDIES; GENETIC PREDISPOSITION TO DISEASE; GESTATIONAL AGE; HAPLOTYPES; HUMANS; INFANT, NEWBORN; INFANT, PREMATURE; INTENSIVE CARE UNITS, NEONATAL; IOWA; MALE; NEONATAL SCREENING; PHENOTYPE; POLYMORPHISM, SINGLE NUCLEOTIDE; RISK FACTORS; THYROID DISEASES; THYROTROPIN;

EID: 84875681310     PISSN: 00313998     EISSN: 15300447     Source Type: Journal    
DOI: 10.1038/pr.2013.18     Document Type: Article

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