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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 - 4 (of 4 Records)

Query Trace: Disease and HAND1[original query]
A functional genetic study identifies HAND1 mutations in septation defects of the human heart.
Human molecular genetics 2009 Oct 18 (19): 3567-78.
Reamon-Buettner Stella Marie, Ciribilli Yari, Traverso Ilaria, Kuhls Beate, Inga Alberto, Borlak Juerg
Investigation of somatic NKX2-5, GATA4 and HAND1 mutations in patients with tetralogy of Fallot.
Pathology 2011 Jun 43 (4): 322-6.
Wang Jian, Lu Yanan, Chen Huiwen, Yin Minzhi, Yu Tingting, Fu Qih
Two novel HAND1 mutations in Chinese patients with ventricular septal defect.
Clinica chimica acta; international journal of clinical chemistry 2012 Apr 413 (7-8): 675-7.
Cheng Zhi, Lib Lin, Li Zhongzhi, Liu Mugen, Yan Jinting, Wang Binbin, Ma
Microdeletions and microduplications in patients with congenital heart disease and multiple congenital anomalies.
Congenital heart disease 0 6 (6): 592-602.
Goldmuntz Elizabeth, Paluru Prasuna, Glessner Joseph, Hakonarson Hakon, Biegel Jaclyn A, White Peter S, Gai Xiaowu, Shaikh Tamim
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