Role of TBX1 in human del22q11.2 syndrome.
By Hisato Yagi, Y. Furutani, H. Hamada, Takashi Sasaki, S. Asakawa, S. Minoshima, F. Ichida, Kunitaka Joo, M. Kimura, S. Imamura and 6 more. The Lancet, 2003
798 citations recorded by the source corpus.
Subfields: Genetics, Molecular Biology
View Paper: https://www.semanticscholar.org/paper/1b6cb843b4344faa09b2439385470d1e81c10879
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Molecular Biology
Citations in the corpus
- The developmental genetics of congenital heart disease (2008, methodology): “This conclusion was supported by the identification of TBX1 missense mutations in patients with features of 22q11 microdeletion syndrome but without a microdeletio”