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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1994 | 1 |
1995 | 1 |
1996 | 2 |
2024 | 0 |
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Page 1
Glanzmann thrombasthenia. Cooperation between sequence variants in cis during splice site selection.
J Clin Invest. 1996 Oct 15;98(8):1745-54. doi: 10.1172/JCI118973.
J Clin Invest. 1996.
PMID: 8878424
Free PMC article.
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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Fifteen novel FBN1 mutations causing Marfan syndrome detected by heteroduplex analysis of genomic amplicons.
Nijbroek G, Sood S, McIntosh I, Francomano CA, Bull E, Pereira L, Ramirez F, Pyeritz RE, Dietz HC.
Nijbroek G, et al.
Am J Hum Genet. 1995 Jul;57(1):8-21.
Am J Hum Genet. 1995.
PMID: 7611299
Free PMC article.
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A molecular approach to the stratification of cardiovascular risk in families with Marfan's syndrome.
Pereira L, Levran O, Ramirez F, Lynch JR, Sykes B, Pyeritz RE, Dietz HC.
Pereira L, et al.
N Engl J Med. 1994 Jul 21;331(3):148-53. doi: 10.1056/NEJM199407213310302.
N Engl J Med. 1994.
PMID: 8008028
Free article.
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