Surfactant protein C gene variation in the Finnish population - Association with perinatal respiratory disease

European Journal of Human Genetics

Volumn 12, Issue 4, 2004, Pages 312-320

  Lahti, Meri ^a   Marttila, Riitta ^b   Hallman, Mikko ^a  

^a UNIVERSITY OF OULU   (Finland)

^b SEINÄJOKI CENTRAL HOSPITAL   (Finland)

Author keywords

Allelic association; Bronchopulmonary dysplasia (BPD); Conformation sensitive gel electrophoresis (CSGE); Genetic polymorphism; Lung surfactant; Respiratory distress syndrome (RDS)

Indexed keywords

DNA; LUNG SURFACTANT; SURFACTANT PROTEIN C;

ARTICLE; CHRONIC LUNG DISEASE; COMPLEX FORMATION; CONTROLLED STUDY; EXON; FEMALE; FINLAND; GEL ELECTROPHORESIS; GENE FREQUENCY; GENE LINKAGE DISEQUILIBRIUM; GENETIC ASSOCIATION; GENETIC POLYMORPHISM; GENETIC SUSCEPTIBILITY; GENETIC VARIABILITY; GENOTYPE; HAPLOTYPE; HUMAN; HYDROPHOBICITY; INFANT; INTERSTITIAL LUNG DISEASE; LUNG ALVEOLUS; LUNG DYSPLASIA; MAJOR CLINICAL STUDY; MALE; MUTATIONAL ANALYSIS; NEONATAL RESPIRATORY DISTRESS SYNDROME; NUCLEOTIDE SEQUENCE; POPULATION GENETICS; PREMATURITY; PRIORITY JOURNAL; RISK FACTOR; SEX DIFFERENCE;

BASE SEQUENCE; BRONCHOPULMONARY DYSPLASIA; DNA PRIMERS; FINLAND; GENETICS, POPULATION; HUMANS; INFANT, NEWBORN; INFANT, PREMATURE; PEPTIDES; POLYMORPHISM, GENETIC; PULMONARY SURFACTANT-ASSOCIATED PROTEIN C; RESPIRATORY DISTRESS SYNDROME, NEWBORN;

EID: 1942440855     PISSN: 10184813     EISSN: None     Source Type: Journal    
DOI: 10.1038/sj.ejhg.5201137     Document Type: Article

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