FOX gene cluster defects in alveolar capillary dysplasia associated with congenital heart disease

Cardiology in the Young

Volumn 23, Issue 5, 2013, Pages 697-704

  Laux, Daniela ^a   Malan, Valérie ^a   Bajolle, Fanny ^a   Boudjemline, Younes ^a   Amiel, Jeanne ^b   Bonnet, Damien ^a  

^a HÔPITAL NECKER ENFANTS MALADES   (France)

^b Clinique de Genetique Medicale   (France)

Author keywords

16q24.1 microdeletion; cardiac malformation; Misalignment of pulmonary veins; neonatal pulmonary hypertension; pulmonary vascular disease

Indexed keywords

TRANSCRIPTION FACTOR;

ALVEOLAR CAPILLARY DYSPLASIA; ARTICLE; ATRIOVENTRICULAR SEPTAL DEFECT; CASE REPORT; CHILD DEATH; CHROMOSOME 16Q; CONGENITAL HEART DISEASE; ECHOCARDIOGRAPHY; FEMALE; FOXF1 GENE; GENE; GENE CLUSTER; GENETIC DISORDER; HEART VENTRICLE SEPTUM DEFECT; HUMAN; INFANT; LUNG BIOPSY; LUNG MALFORMATION; LUNG VASCULAR RESISTANCE; MALE; MEDICAL RECORD REVIEW; RECIPROCAL CHROMOSOME TRANSLOCATION;

CHROMOSOMES, HUMAN, PAIR 16; FEMALE; FORKHEAD TRANSCRIPTION FACTORS; HEART SEPTAL DEFECTS; HEART SEPTAL DEFECTS, VENTRICULAR; HUMANS; INFANT, NEWBORN; MALE; MULTIGENE FAMILY; PERSISTENT FETAL CIRCULATION SYNDROME; PULMONARY ALVEOLI; RETROSPECTIVE STUDIES; TRANSLOCATION, GENETIC;

EID: 84883405454     PISSN: 10479511     EISSN: 14671107     Source Type: Journal    
DOI: 10.1017/S1047951112001904     Document Type: Article

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