Delineating the Hemostaseome as an aid to individualize the analysis of the hereditary basis of thrombotic and bleeding disorders-Reference-Cited by-同舟云学术

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Delineating the Hemostaseome as an aid to individualize the analysis of the hereditary basis of thrombotic and bleeding disorders

Published:2011-05-03 Issue:1 Volume:130 Page:149-166
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Fechtel Kim,Osterbur Marika L.,Kehrer-Sawatzki Hildegard,Stenson Peter D.,Cooper David N.

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/s00439-011-0984-y.pdf

Reference89 articles.

1. ACOG Committee Opinion (2009) ACOG Committee Opinion no. 451: Von Willebrand disease in women. Obstet Gynecol 114:1439–1443. doi: 10.1097/AOG.0b013e3181c6f975

2. Arellano AR, Bezemer ID, Tong CH, Catanese JJ, Devlin JJ, Reitsma PH, Bare LA, Rosendaal FR (2010) Gene variants associated with venous thrombosis: confirmation in the MEGA study. J Thromb Haemost 8:1132–1134. doi: 10.1111/j.1538-7836.2010.03782.x

3. Asatiani E, Kessler CM (2007) Multiple congenital coagulopathies co-expressed with von Willebrand’s disease: the experience of Hemophilia Region III Treatment Centers over 25 years and review of the literature. Haemophilia 13:685–696. doi: 10.1111/j.1365-2516.2007.01541.x

4. Ashley EA, Butte AJ, Wheeler MT, Chen R, Klein TE, Dewey FE, Dudley JT, Ormond KE, Pavlovic A, Morgan AA, Pushkarev D, Neff NF, Hudgins L, Gong L, Hodges LM, Berlin DS, Thorn CF, Sangkuhl K, Hebert JM, Woon M, Sagreiya H, Whaley R, Knowles JW, Chou MF, Thakuria JV, Rosenbaum AM, Zaranek AW, Church GM, Greely HT, Quake SR, Altman RB (2010) Clinical assessment incorporating a personal genome. Lancet 375:1525–1535. doi: 10.1016/S0140-6736(10)60452-7

5. Astermark J, Tengborn L, Hedner U, Berntorp E (2001) Anti- and procoagulant activities in factor VII-deficient subjects. Thromb Res 101:435–440

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