Relation of genotype 22q11 deletion to phenotype of pulmonary vessels in tetralogy of Fallot and pulmonary atresia-ventricular septal defect

Objective—To compare the morphology of the pulmonary vessels in tetralogy of Fallot or pulmonary atresia-ventricular septal defect (PA-VSD) with (del22q) and without 22q11 deletion (non-del22q).
Patients—94 consecutive infants (54 with tetralogy of Fallot, 40 with PA-VSD) were studied using ultrasou...

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Detalhes bibliográficos
Main Authors: Chessa, M, Butera, G, Bonhoeffer, P, Iserin, L, Kachaner, J, Lyonnet, S, Munnich, A, Sidi, D, Bonnet, D
Formato: Artigo
Idioma:Inglês
Publicado em: 1998
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Papers
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1728608/
https://ncbi.nlm.nih.gov/pubmed/9538314
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