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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 5 (of 5 Records)

Query Trace: Disease and CFC1[original query]
CFC1 mutations in patients with transposition of the great arteries and double-outlet right ventricle.
American journal of human genetics 2002 1 70 (3): 776-80.
Goldmuntz Elizabeth, Bamford Richard, Karkera Jayaprakash D, dela Cruz June, Roessler Erich, Muenke Maximili
Mutations in the EGF-CFC gene cryptic are an infrequent cause of congenital heart disease.
Pediatric cardiology 0 27 (6): 695-8.
Ozcelik Cemil, Bit-Avragim Nana, Panek Anna, Gaio Ursula, Geier Christian, Lange Peter E, Dietz Rainer, Posch Maximilian G, Perrot Andreas, Stiller Brigit
Variants of the CFC1 gene in patients with laterality defects associated with congenital cardiac disease.
Cardiology in the young 2007 Jun 17 (3): 268-74.
Selamet Tierney Elif Seda, Marans Zvi, Rutkin Melissa B, Chung Wendy
CFC1 mutations in Chinese children with congenital heart disease.
International journal of cardiology 2011 Jan 146 (1): 86-8.
Wang Binbin, Wang Jing, Liu Shiguo, Han Xiaoyang, Xie XiaoDong, Tao You, Yan Jinting, Ma
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
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