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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1993 | 1 |
1996 | 1 |
1997 | 3 |
2024 | 0 |
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Page 1
The pathogenicity of the Pro1148Ala substitution in the FBN1 gene: causing or predisposing to Marfan syndrome and aortic aneurysm, or clinically innocent?
Hum Genet. 1997 May;99(5):607-11. doi: 10.1007/s004390050414.
Hum Genet. 1997.
PMID: 9150726
P1148A in fibrillin-1 is not a mutation anymore.
Wang M, Mathews KR, Imaizumi K, Beiraghi S, Blumberg B, Scheuner M, Graham JM Jr, Godfrey M.
Wang M, et al.
Nat Genet. 1997 Jan;15(1):12. doi: 10.1038/ng0197-12.
Nat Genet. 1997.
PMID: 8988160
No abstract available.
Item in Clipboard
Mutation screening of complete fibrillin-1 coding sequence: report of five new mutations, including two in 8-cysteine domains.
Tynan K, Comeau K, Pearson M, Wilgenbus P, Levitt D, Gasner C, Berg MA, Miller DC, Francke U.
Tynan K, et al.
Hum Mol Genet. 1993 Nov;2(11):1813-21. doi: 10.1093/hmg/2.11.1813.
Hum Mol Genet. 1993.
PMID: 8281141
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Mutation in fibrillin-1 and the Marfanoid-craniosynostosis (Shprintzen-Goldberg) syndrome.
Sood S, Eldadah ZA, Krause WL, McIntosh I, Dietz HC.
Sood S, et al.
Nat Genet. 1996 Feb;12(2):209-11. doi: 10.1038/ng0296-209.
Nat Genet. 1996.
PMID: 8563763
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P1148A in fibrillin-1 is not a mutation leading to Shprintzen-Goldberg syndrome.
Watanabe Y, Yano S, Koga Y, Yukizane S, Nishiyori A, Yoshino M, Kato H, Ogata T, Adachi M.
Watanabe Y, et al.
Hum Mutat. 1997;10(4):326-7. doi: 10.1002/(SICI)1098-1004(1997)10:4<326::AID-HUMU10>3.0.CO;2-1.
Hum Mutat. 1997.
PMID: 9338588
No abstract available.
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