Tricuspid Atresia
What's New
Last Posted: Nov 07, 2015
- Genetic mutation analysis in Japanese patients with non-syndromic congenital heart disease.
Yoshida Akiko, et al. Journal of human genetics 2015 10 - The Association of H1N1 Pandemic Influenza with Congenital Anomaly Prevalence in Europe: An Ecological Time Series Study.
Luteijn Johannes Michiel, et al. Epidemiology (Cambridge, Mass.) 2015 8 - Tricuspid atresia
From NCATS Genetic and Rare Diseases Information Center - Differential duplication of an intronic region in the NFATC1 gene in patients with congenital heart disease.
Yehya Amin, et al. Genome / National Research Council Canada = Génome / Conseil national de recherches Canada 2006 9 (9) 1092-8 - ZFPM2/FOG2 and HEY2 genes analysis in nonsyndromic tricuspid atresia.
Sarkozy Anna, et al. American journal of medical genetics. Part A 2005 2 (1) 68-70
Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
- Eclampsia
- Erythema Multiforme
- Familial Mediterranean Fever
- Fragile X Syndrome
- Gaucher Disease
- Glomerulonephritis
- Graves Disease
- Hemophilia
- Huntington Disease
- Microcephaly
- Myasthenia Gravis
- Phenylketonuria
- Retinitis Pigmentosa
- Severe Combined Immunodeficiency
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- Page last reviewed:Feb 1, 2024
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