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Información de la revista
Vol. 52. Núm. 5.
Páginas 485-487 (mayo 2000)
Vol. 52. Núm. 5.
Páginas 485-487 (mayo 2000)
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La resonancia magnética en un recién nacido con agenesia de válvula pulmonar y deleción del cromosoma 22q 11,2
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Biblografía
[1.]
N. Chevers.
Recherches sur les maladies de l'artère pulmonaire.
Arch Gen Med, 15 (1847), pp. 488-508
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Le agenesie des valves pulmonaires. Experience sur 20 annes.
Arch Mal Coeur, 88 (1995), pp. 673-679
[3.]
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A genetic etiology for DiGeorge syndrome: Consistent deletion and microdeletion of 22q11.
Am J Hum Genet, 50 (1992), pp. 924-933
[4.]
P.Y. Scambler, D. Kelly, E. Lindsay, R. Willianson, R. Goldberg, R. Shprintzen, et al.
Velo-cardio-facial syndrome associated with chromosome 22 deletions encompassing the DiGeorge locus.
Lancet, 339 (1992), pp. 1138-1139
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E. Goldmunta, D.A. Driscoll, M.L. Budarf, E.M. Zackai, D.M. McDonal-McGinn, J.A. Biegel, et al.
Microdeletion of chromosomal region 22q11 in infant with congenital cardiac defects.
J Med Genet, 30 (1993), pp. 807-812
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Prenatal diagnosis and circulatory characteristics in tetralogy of Fallot with absent pulmonary valve.
Am J Cardiol, 64 (1989), pp. 547-549
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Magnetic resonance imaging of absent pulmonary valve syndrome.
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Deletion within chromosome 22q11 in familial congenital heart disease.
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Interstitial deletion of the long arm of chromosome 6 associated with absent pulmonary valve.
Am J Med Genet, 38 (1991), pp. 608-611
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Congenital absence of pulmonary valve associated with tetralogy of Fallot: Diagnosis by 2-dimensional echocardiography.
Am J Cardiol, 51 (1983), pp. 1789-1800
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