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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Sep 8, 2024. (Total: 231257Documents)
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Records 1 - 3 (of 3 Records)

Query Trace: Marfan Syndrome and SMAD3[original query]
Application of next-generation sequencing to screen for pathogenic mutations in 123 unrelated Chinese patients with Marfan syndrome or a related disease.
Science China. Life sciences 2019 5 62 (12): 1630-1637.
Li Jiacheng, Lu Chaoxia, Wu Wei, Liu Yaping, Wang Rongrong, Si Nuo, Meng Xiaolu, Zhang Shuyang, Zhang X
Genetic basis of hereditary thoracic aortic aneurysms and dissections.
Journal of cardiology 2019 4 74 (2): 136-143.
Takeda Norifumi, Komuro Iss
Optimising the mutation screening strategy in Marfan syndrome and identifying genotypes with more severe aortic involvement.
Orphanet journal of rare diseases 2020 Oct 15 (1): 290.
Stengl Roland, Bors András, Ágg Bence, Pólos Miklós, Matyas Gabor, Molnár Mária Judit, Fekete Bálint, Csabán Dóra, Andrikovics Hajnalka, Merkely Béla, Radovits Tamás, Szabolcs Zoltán, Benke Kálm
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