Dominant mode of inheritance in atrial septal defect
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1971.tb00259.x/fullpdf
Reference39 articles.
1. Congenital heart disease with arrhythmia in a family;Amarasingham;Brit. Heart J.,1967
2. Chromosome studies in 156 patients with congenital heart disease;Anders;Brit. Heart J.,1965
3. Familial atrial septal defect with prolonged atrioventricular conduction;Bizarro;Circulation,1970
4. Association between congenital heart malformation and chromosomal variations;Böök;Acta paediat. scand.,1961a
5. Translocation heterozygosity in man;Böök;Lancet,1961b
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2. Familial atrial septal defect in the oval fossa with progressive prolongation of the atrioventricular conduction caused by mutations in the NKX2.5 gene;Cardiology in the Young;2008-12-02
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