Evaluation of fetal and maternal genetic variation in the progesterone receptor gene for contributions to preterm birth

Pediatric Research

Volumn 62, Issue 5, 2007, Pages 630-635

  Ehn, Nicole L ^a   Cooper, Margaret E ^b   Orr, Kristin ^a   Shi, Min ^c   Johnson, Marla K ^a   Caprau, Diana ^a   Dagle, John ^a   Steffen, Katherine ^a   Johnson, Karen ^a   Marazita, Mary L ^b   Merrill, David ^d   Murray, Jeffrey C ^a  

^a UNIVERSITY OF IOWA   (United States)

^b UNIVERSITY OF PITTSBURGH   (United States)

^c NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES   (United States)

^d WAKE FOREST SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; PROGESTERONE RECEPTOR;

ARTICLE; DNA SEQUENCE; FATHER; GENE; GENE DELETION; GENE INSERTION; GENE LINKAGE DISEQUILIBRIUM; GENETIC ANALYSIS; GENETIC ASSOCIATION; GENETIC IDENTIFICATION; GENETIC VARIABILITY; HUMAN; LOGLINEAR MODEL; MAJOR CLINICAL STUDY; MOTHER; NEWBORN; PREMATURE LABOR; PREMATURITY; PRIORITY JOURNAL; PROGESTERONE RECEPTOR GENE; SINGLE NUCLEOTIDE POLYMORPHISM; UNITED STATES; EVALUATION; FEMALE; GENE EXPRESSION REGULATION; GENE FREQUENCY; GENETIC PREDISPOSITION; GENETICS; GESTATIONAL AGE; INSERTION DELETION MUTATION; MALE; NUCLEOTIDE SEQUENCE; PREGNANCY; REGISTER; RISK ASSESSMENT; RISK FACTOR;

DNA MUTATIONAL ANALYSIS; FEMALE; GENE EXPRESSION REGULATION, DEVELOPMENTAL; GENE FREQUENCY; GENETIC PREDISPOSITION TO DISEASE; GESTATIONAL AGE; HUMANS; INDEL MUTATION; INFANT, NEWBORN; INFANT, PREMATURE; MALE; POLYMORPHISM, SINGLE NUCLEOTIDE; PREGNANCY; PREMATURE BIRTH; RECEPTORS, PROGESTERONE; REGISTRIES; RISK ASSESSMENT; RISK FACTORS;

EID: 38849117244     PISSN: 00313998     EISSN: None     Source Type: Journal    
DOI: 10.1203/PDR.0b013e3181567bfc     Document Type: Article

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