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Year | Number of Results |
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2003 | 1 |
2015 | 1 |
2018 | 1 |
2024 | 0 |
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Role of TBX1 in human del22q11.2 syndrome.
Lancet. 2003 Oct 25;362(9393):1366-73. doi: 10.1016/s0140-6736(03)14632-6.
Lancet. 2003.
PMID: 14585638
A Novel TBX1 Loss-of-Function Mutation Associated with Congenital Heart Disease.
Pan Y, Wang ZG, Liu XY, Zhao H, Zhou N, Zheng GF, Qiu XB, Li RG, Yuan F, Shi HY, Hou XM, Yang YQ.
Pan Y, et al.
Pediatr Cardiol. 2015 Oct;36(7):1400-10. doi: 10.1007/s00246-015-1173-x. Epub 2015 Apr 10.
Pediatr Cardiol. 2015.
PMID: 25860641
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Whole exome sequencing identifies mutations in 10% of patients with familial non-syndromic cleft lip and/or palate in genes mutated in well-known syndromes.
Basha M, Demeer B, Revencu N, Helaers R, Theys S, Bou Saba S, Boute O, Devauchelle B, Francois G, Bayet B, Vikkula M.
Basha M, et al.
J Med Genet. 2018 Jul;55(7):449-458. doi: 10.1136/jmedgenet-2017-105110. Epub 2018 Mar 2.
J Med Genet. 2018.
PMID: 29500247
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