HuGE Literature Finder
Records 1-2
Study of six patients with complete F9 deletion characterized by cytogenetic microarray: role of the SOX3 gene in intellectual disability.
Journal of thrombosis and haemostasis : JTH 2016 Oct 14 (10): 1988-1993. Jourdy Y, Chatron N, Carage M-L, Fretigny M, Meunier S, Zawadzki C, Gay V, Negrier C, Sanlaville D, Vinciguerra |
F9 Malmö, factor IX and deep vein thrombosis.
Haematologica 2009 May 94 (5): 693-9. Bezemer Irene D, Arellano Andre R, Tong Carmen H, Rowland Charles M, Ireland Helen A, Bauer Kenneth A, Catanese Joseph, Reitsma Pieter H, Doggen Carine J M, Devlin James J, Rosendaal Frits R, Bare Lance |
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