Human Genome Epidemiology Literature Finder
Rare Diseases
Records 1 - 3 (of 3 Records) |
Query Trace: Dextrocardia[original query] |
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[Mutation analysis of Cited2 in patients with congenital heart disease]. Zhonghua er ke za zhi. Chinese journal of pediatrics 2010 Apr 48 (4): 293-6. Yang Xiao-fei, Wu Xiao-yun, Li Mi, Li Yong-gang, Dai Jiang-tao, Bai Yong-hong, Tian J |
NPHP4 variants are associated with pleiotropic heart malformations. Circulation research 2012 Jun 110 (12): 1564-74. French Vanessa M, van de Laar Ingrid M B H, Wessels Marja W, Rohe Christan, Roos-Hesselink Jolien W, Wang Guangliang, Frohn-Mulder Ingrid M E, Severijnen Lies-Anne, de Graaf Bianca M, Schot Rachel, Breedveld Guido, Mientjes Edwin, van Tienhoven Marianne, Jadot Elodie, Jiang Zhengxin, Verkerk Annemieke, Swagemakers Sigrid, Venselaar Hanka, Rahimi Zohreh, Najmabadi Hossein, Meijers-Heijboer Hanne, de Graaff Esther, Helbing Wim A, Willemsen Rob, Devriendt Koen, Belmont John W, Oostra Ben A, Amack Jeffrey D, Bertoli-Avella Aida |
Autosomal dominant nanophthalmos and high hyperopia associated with a C-terminal frameshift variant in MYRF. Molecular vision 2019 11 25 527-534. Siggs Owen M, Souzeau Emmanuelle, Breen James, Qassim Ayub, Zhou Tiger, Dubowsky Andrew, Ruddle Jonathan B, Craig Jamie |
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- Page last updated:Apr 22, 2024
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