Developmental and genetic aspects of congenital diaphragmatic hernia

Pediatric Pulmonology

Volumn 47, Issue 6, 2012, Pages 534-545

  Veenma, D C M ^a   De Klein, A ^a   Tibboel, D ^a  

^a SOPHIA CHILDREN S HOSPITAL   (Netherlands)

Author keywords

alternative retinoid signaling disturbance; congenital diaphragmatic hernia; diaphragm embryology; molecular genetic pathways

Indexed keywords

CHROMOSOME ABERRATION; CLINICAL FEATURE; CONGENITAL DIAPHRAGM HERNIA; CYTOGENETICS; DISEASE ASSOCIATION; DNA DETERMINATION; EMBRYO DEVELOPMENT; GENETIC ANALYSIS; GENETIC SUSCEPTIBILITY; HUMAN; HYPOTHESIS; LUNG HYPOPLASIA; MESENCHYME; MOLECULAR GENETICS; NEONATAL RESPIRATORY DISTRESS SYNDROME; NONHUMAN; PATHOGENESIS; PRENATAL EXPOSURE; PRIORITY JOURNAL; PROGNOSIS; PULMONARY HYPERTENSION; REVIEW; SIGNAL TRANSDUCTION; TREATMENT OUTCOME;

DIAPHRAGM; GENETIC PREDISPOSITION TO DISEASE; HERNIA, DIAPHRAGMATIC; HUMANS; INFANT, NEWBORN; LUNG;

EID: 84861228019     PISSN: 87556863     EISSN: 10990496     Source Type: Journal    
DOI: 10.1002/ppul.22553     Document Type: Review

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