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Volumn 39, Issue 8, 2015, Pages 568-573

What is the basis for a genetic approach in neonatal disorders?

Author keywords

Apnea of prematurity; BPD; IVH; NEC; Neonatal sepsis; PDA; Premature newborn; RDS; ROP; Twin studies

Indexed keywords

BRAIN HEMORRHAGE; GENETIC ANALYSIS; GENOTYPE ENVIRONMENT INTERACTION; HERITABILITY; HUMAN; LUNG DYSPLASIA; NECROTIZING ENTEROCOLITIS; NEONATAL RESPIRATORY DISTRESS SYNDROME; NEWBORN APNEA; NEWBORN DISEASE; NEWBORN SEPSIS; NONHUMAN; PATENT DUCTUS ARTERIOSUS; PHENOTYPE; PREMATURITY; PRIORITY JOURNAL; RETROLENTAL FIBROPLASIA; REVIEW; SINGLE NUCLEOTIDE POLYMORPHISM; TWINS; ADAPTIVE IMMUNITY; BREAST MILK; BRONCHOPULMONARY DYSPLASIA; DRUG EFFECTS; ENTEROCOLITIS, NECROTIZING; FEMALE; GENETICS; IMMUNOLOGY; INFANT; INFANT MORTALITY; INTERMITTENT POSITIVE PRESSURE VENTILATION; MALE; NEWBORN; NEWBORN INTENSIVE CARE; PRACTICE GUIDELINE; PREGNANCY; RESPIRATORY DISTRESS SYNDROME, NEWBORN; RETINOPATHY OF PREMATURITY; SEPSIS; TIME FACTOR; TREATMENT OUTCOME;

EID: 84946731339     PISSN: 01460005     EISSN: 1558075X     Source Type: Journal    
DOI: 10.1053/j.semperi.2015.09.003     Document Type: Review
Times cited : (9)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.