| 1 | FBN1, WMSAD
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| Cervical artery dissection expands the cardiovascular phenotype in FBN1-related Weill-Marchesani syndrome.
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| Newell K, Smith W, Ghoshhajra B, Isselbacher E, Lin A, Lindsay ME.
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| Am J Med Genet A 173(9):2551-2556. doi: 10.1002/ajmg.a.38353. Epub 2017 Jul 11.
2017
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| 2 | ADAMTS10, FBN1, WMSAD, WMSAR
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| ADAMTS10 protein interacts with fibrillin-1 and promotes its deposition in extracellular matrix of cultured fibroblasts.
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| Kutz WE, Wang LW, Bader HL, Majors AK, Iwata K, Traboulsi EI, Sakai LY, Keene DR, Apte SS.
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| J Biol Chem 286(19):17156-67. Epub 2011 Mar 14.
2011
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| 3 | FBN1, TGFBR1, TGFBR2, ECTL, MFS1, TAA, WMSAD, CCSND1, CCSND2, FRLS
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| Recent progress in genetics of Marfan syndrome and Marfan-associated disorders.
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| Mizuguchi T, Matsumoto N.
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| J Hum Genet 52(1):1-12. Epub 2006 Oct 24. Review. 2007
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| 4 | WMSAD, WMSAR
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| Cardiac findings in Weill-Marchesani syndrome.
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| Kojuri J, Razeghinejad MR, Aslani A.
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| Am J Med Genet A 143(17):2062-4. No abstract available. 2007
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| 5 | FBN1, WMSAD
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| In frame fibrillin-1 gene deletion in autosomal dominant Weill-Marchesani syndrome.
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| Faivre L, Gorlin RJ, Wirtz MK, Godfrey M, Dagoneau N, Samples JR, Le Merrer M, Collod-Beroud G, Boileau C, Munnich A, Cormier-Daire V.
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| J Med Genet 40(1):34-6. 2003
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| 6 | WMSAD
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| Exclusion of chromosome 15q21.1 in autosomal-recessive Weill-Marchesani syndrome in an inbred Lebanese family.
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| Megarbane A, Mustapha M, Bleik J, Waked N, Delague V, Loiselet J.
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| Clin Genet 58(6):473-8. 2000
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| 7 | WMSAD
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| Weill-Marchesani syndrome - possible linkage of the autosomal dominant form to 15q21.1.
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| Wirtz MK, et al.
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| Am J Med Genet 65 : 68-75. 1996
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| 8 | WMSAD, FBN1
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| Weill-Marchesani syndrome--possible linkage of the autosomal dominant form to 15q21.1.
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| Wirtz MK, Samples JR, Kramer PL, Rust K, Yount J, Acott TS, Koler RD,Cisler J, Jahed A, Gorlin RJ, Godfrey M.
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| Am J Med Genet 65(1):68-75. 1996
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