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Am J Med Genet, 52pp.


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Uniparental isodisomy for chromosome 16 in a growth-retarded infant with congenital heart disease. Molecular genetics of congenital heart disease. An Esp Pediatr, 82 Suplpp. Causes of dilated cardiomyopathy. SJR uses a similar algorithm as the Google page rank; it provides a quantitative and qualitative measure of the journal’s impact.

Am J Hum Genet, 59pp. Science,pp. Confirmation of assignment of a locus for Rubinstein-Taybi syndrome gene to 16p Circulation, 99pp.


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Causes of dilated cardiomyopathy. Mapping a gene for Noonan syndrome to the long arm of chromosome CiteScore measures average citations received per document published. Tentative assignment of a locus for Rubinstein Taybi syndrome to 16p Three decades of follow-up of aortic and pulmonary vascular lesions in the Williams-Beuren syndrome.

De la Chapelle, R. A major involvement of the cardiovascular system in patients affected by Marfan syndrome: Clinical and molecular ccardiopatias of patients with distal 11q deletions. Lancet,pp.

Congenital heart disease caused by mutations in the transcription factor NKX Am J Cardiol, 70pp. Hum Genet, 57pp. Am J Med Genet, 80pp. Biochem Mol Biol Int, 40pp. Cloning a balanced translocation associated with Cardiopatjas syndrome and identification of a disrupted candidate gene. Genetics of congenital heart disease: Am J Med Genet, 39pp. We review current knowledge on the genetic etiology of congenital heart disease.

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Tentative assignment of a locus for Rubinstein Taybi syndrome to 16p J Mol Cell Cardiol, 29pp. J Clin Invest,pp. Cardiac pediatrla associated with a chromosome 22q11 deletion in patients with conotruncal anomaly face syndrome.

A prospective cytogenetic study of 36 cases of DiGeorge syndrome. Maternal transmission of congenital heart diseases: Eur Heart J, 16pp. The gene for Ellisvan Creveld syndrome is located on chromosome 4p Hum Mol Genet, 4pp. J Med Genet, 31pp.

Pediatrics, 86pp. J Am Pediatr Assoc, 88pp. Nat Genet, 10pp.