FUT 2 polymorphism and outcome in very-low-birth-weight infants

Pediatric Research

Volumn 77, Issue 4, 2015, Pages 586-590

  Demmert, Martin ^a   Schaper, Anne ^a   Pagel, Julia ^a   Gebauer, Corinna ^b   Emeis, Michael ^c   Heitmann, Friedhelm ^d   Kribs, Angela ^e   Siegel, Jens ^f   Müller, Dirk ^g   Keller Wackerbauer, Annette ^h   Gerleve, Hubert ⁱ   Wieg, Christian ^j   Herting, Egbert ^a   Göpel, Wolfgang ^a   Härtel, Christoph ^a  

^a UNIVERSITY OF LÜBECK   (Germany)

^b UNIVERSITY OF LEIPZIG   (Germany)

^c VIVANTES KLINIKUM NEUKÖLLN   (Germany)

^d KLINIKUM DORTMUND   (Germany)

^e UNIVERSITY OF COLOGNE   (Germany)

^f Children's Hospital Auf der Bult   (Germany)

^g KLINIKUM KASSEL   (Germany)

^h KRANKENHAUS BARMHERZIGE BRÜDER   (Germany)

ⁱ Department of Neonatology Klinikum Coesfeld   (Germany)

^j KLINIKUM ASCHAFFENBURG   (Germany)

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Author keywords

[No Author keywords available]

Indexed keywords

DNA; FUCOSYLTRANSFERASE; GALACTOSIDE 2-ALPHA-L-FUCOSYLTRANSFERASE;

ADVERSE OUTCOME; ARTICLE; BRAIN HEMORRHAGE; COHORT ANALYSIS; CONTROLLED STUDY; DNA EXTRACTION; FEMALE; FUCOSYLTRANSFERASE 2 GENE; GENE; GENE MUTATION; GENETIC ASSOCIATION; GENETIC MODEL; GENOTYPE; HUMAN; INCIDENCE; INFANT; INTESTINE PERFORATION; MAJOR CLINICAL STUDY; MALE; NECROTIZING ENTEROCOLITIS; NEWBORN SEPSIS; ORAL BIOPSY; POPULATION BASED CASE CONTROL STUDY; PREDICTOR VARIABLE; PREMATURITY; PRIORITY JOURNAL; PROSPECTIVE STUDY; RECESSIVE INHERITANCE; SINGLE NUCLEOTIDE POLYMORPHISM; VERY LOW BIRTH WEIGHT; VULNERABLE POPULATION; ABNORMALITIES; CLINICAL TRIAL; GENETIC POLYMORPHISM; GENETIC PREDISPOSITION; GENETICS; INTESTINE; MULTICENTER STUDY; NEWBORN; RECESSIVE GENE; SEPSIS;

CEREBRAL HEMORRHAGE; ENTEROCOLITIS, NECROTIZING; FEMALE; FUCOSYLTRANSFERASES; GENES, RECESSIVE; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; HUMANS; INFANT; INFANT, NEWBORN; INFANT, PREMATURE; INFANT, PREMATURE, DISEASES; INFANT, VERY LOW BIRTH WEIGHT; INTESTINAL PERFORATION; INTESTINES; MALE; POLYMORPHISM, GENETIC; PROSPECTIVE STUDIES; SEPSIS;

EID: 84924967767     PISSN: 00313998     EISSN: 15300447     Source Type: Journal    
DOI: 10.1038/pr.2015.1     Document Type: Article

References (18)

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