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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1996 | 2 |
1997 | 3 |
2000 | 1 |
2024 | 0 |
Search Results
6 results
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Page 1
Partial cloning and sequencing of chick fibrillin-1 cDNA.
In Vitro Cell Dev Biol Anim. 2000 Jan;36(1):19-25. doi: 10.1290/1071-2690(2000)036<0019:pcasoc>2.0.co;2.
In Vitro Cell Dev Biol Anim. 2000.
PMID: 10691037
Prenatal diagnosis in congenital contractural arachnodactyly.
Belleh S, Spooner L, Allanson J, Godfrey M.
Belleh S, et al.
Genet Test. 1997-1998;1(4):293-6. doi: 10.1089/gte.1997.1.293.
Genet Test. 1997.
PMID: 10464661
Item in Clipboard
Three novel fibrillin mutations in exons 25 and 27: classic versus neonatal Marfan syndrome.
Wang M, Wang JY, Cisler J, Imaizumi K, Burton BK, Jones MC, Lamberti JJ, Godfrey M.
Wang M, et al.
Hum Mutat. 1997;9(4):359-62. doi: 10.1002/(SICI)1098-1004(1997)9:4<359::AID-HUMU10>3.0.CO;2-1.
Hum Mutat. 1997.
PMID: 9101298
No abstract available.
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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.
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Delivery of a hammerhead ribozyme specifically down-regulates the production of fibrillin-1 by cultured dermal fibroblasts.
Kilpatrick MW, Phylactou LA, Godfrey M, Wu CH, Wu GY, Tsipouras P.
Kilpatrick MW, et al.
Hum Mol Genet. 1996 Dec;5(12):1939-44. doi: 10.1093/hmg/5.12.1939.
Hum Mol Genet. 1996.
PMID: 8968747
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Weill-Marchesani syndrome--possible linkage of the autosomal dominant form to 15q21.1.
Wirtz MK, Samples JR, Kramer PL, Rust K, Yount J, Acott TS, Koler RD, Cisler J, Jahed A, Gorlin RJ, Godfrey M.
Wirtz MK, et al.
Am J Med Genet. 1996 Oct 2;65(1):68-75. doi: 10.1002/(SICI)1096-8628(19961002)65:1<68::AID-AJMG11>3.0.CO;2-P.
Am J Med Genet. 1996.
PMID: 8914744
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