Human Genome Epidemiology Literature Finder
Rare Diseases
Records 1 - 4 (of 4 Records) |
Query Trace: Tricuspid Atresia[original query] |
---|
ZFPM2/FOG2 and HEY2 genes analysis in nonsyndromic tricuspid atresia. American journal of medical genetics. Part A 2005 Feb 133A (1): 68-70. Sarkozy Anna, Conti Emanuela, D'Agostino Rita, Digilio Maria Cristina, Formigari Roberto, Picchio Fernando, Marino Bruno, Pizzuti Antonio, Dallapiccola Bru |
Differential duplication of an intronic region in the NFATC1 gene in patients with congenital heart disease. Genome / National Research Council Canada = Génome / Conseil national de recherches Canada 2006 Sep 49 (9): 1092-8. Yehya Amin, Souki Ramzi, Bitar Fadi, Nemer Georg |
The Association of H1N1 Pandemic Influenza with Congenital Anomaly Prevalence in Europe: An Ecological Time Series Study. Epidemiology (Cambridge, Mass.) 2015 Aug . Luteijn Johannes Michiel, Addor Marie-Claude, Arriola Larraitz, Bianchi Fabrizio, Garne Ester, Khoshnood Babak, Nelen Vera, Neville Amanda, Queisser-Luft Annette, Rankin Judith, Rounding Catherine, Verellen-Dumoulin Christine, de Walle Hermien, Wellesley Diana, Wreyford Ben, Yevtushok Lyubov, de Jong-van den Berg Lolkje, Morris Joan, Dolk Hel |
Genetic mutation analysis in Japanese patients with non-syndromic congenital heart disease. Journal of human genetics 2015 Oct . Yoshida Akiko, Morisaki Hiroko, Nakaji Mai, Kitano Masataka, Kim Ki-Sung, Sagawa Koichi, Ishikawa Shiro, Satokata Ichiro, Mitani Yoshihide, Kato Hitoshi, Hamaoka Kenji, Echigo Shigeyuki, Shiraishi Isao, Morisaki Takayu |
- Page last reviewed:Feb 1, 2024
- Content source: