Evaluación Radiológica de las Cardiopatias Congenitas. 1. Cardiopatías Congénitas; 2. Cardiopatías Congénitas Incidencia 8 de cada. Primer sitio Web en Argentina sobre cardiopatías congénitas.

Author: Kigagrel Gogrel
Country: Saudi Arabia
Language: English (Spanish)
Genre: Literature
Published (Last): 27 February 2008
Pages: 428
PDF File Size: 11.30 Mb
ePub File Size: 10.39 Mb
ISBN: 636-4-46404-697-7
Downloads: 76186
Price: Free* [*Free Regsitration Required]
Uploader: Shaktitaur

Cardiac anomalies associated with a chromosome 22q11 deletion in patients with conotruncal anomaly face syndrome. Confirmation of assignment of a locus for Rubinsten-Taybi syndrome gene to 16p Hum Genet, 65pp. Mapping of microsatellite markers in the Alagille region and screening of microdeletions by genotyping 23 patients. Submicroscopic deletions at 16p Recent progress in the molecular genetics of congenital heart defects. J Pediatr,pp.

The DiGeorge anomaly with renal agenesis in infants of mothers with diabetes. Arch Dis Child, 71pp.


Continuing navigation will be considered as acceptance of this use. The gene for Ellisvan Creveld syndrome is located on chromosome 4p Mapping a gene for Noonan syndrome to the long arm of chromosome The association of the DiGeorge anomaly with partial monosomy of chromosome Ultrasound Obstetr Gynecol, 10pp.


Am J Med Genet, 29pp. The genetic basis of paediatric cardiovascular disease. A common region of 10p deleted in DiGeorge and velocardiofacial syndromes. Am J Med Genet, 83pp. J Am Coll Cardiol, 23pp. Am J Med Genet, 73pp. The DiGeorge anomaly as a pediatri field defect.

Cafdiopatias J Med Genet, 44pp.


Am J Med Genet, 37pp. Deletions of 20p12 in Alagille syndrome: J Pediatr,pp.

Myocardial infartation leading to sudden death in the Williams syndrome: J Am Coll Cardiol, 23pp. Eur Heart J, 16pp.

Am J Med Genet, 46pp. Prenat Diagn, 15pp. J Med Genet, 30pp. Mapping a gene for Noonan syndrome to the long arm of chromosome Am J Med Genet, 80pp. Cell, 73pp. An Esp Pediatr, 82 Suplpp.

Mitochondrial inheritance and chromosomal anomalies can cardiiopatias be responsible for congenital heart malformations.

Envianos tu consulta

Tentative assignment of a locus for Rubinstein Taybi syndrome to 16p Prevalence of 22q11 microdeletions in Di-George and velocardiofacial syndromes: Nat Genet, 13pp. Recurrence risk in offspring of adults with dn heart defects: A search for chromosome 22q Van der Burgt, A.


Hypoparathyroidism as the major manifestation in two patients with 22q11 deletions. Ann Med, 27pp.

The compulsion of chirality: Am J Med Genet, 47 Suplpp.