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Entries: 1-4  
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[Abstract] A founder effect for p47 Trp193X CGD?
Authors: de Boer, M.; van Leeuwen, K.; Tzur, S.; Yudkovsky, G.; Skorecki, K.; Wolach, B.; Gavrieli, R.; Nasidze, Ivan; Stoneking, Mark; van den Berg, T. K.; Roos, D.
Date of Publication (YYYY-MM-DD): 2011
Name of Conference/Meeting: 45th Annual Scientific Meeting of the European Society for Clinical Investigation
Title of Journal: European Journal of Clinical Investigation
Volume (in Journal): 41
Issue / Number: s1
Start Page: 41
End Page: 41
Document Type: Conference-Paper
ID: 572045.0
LAD-1/variant syndrome is caused by mutations in FERMT3
Authors: Kuijpers, T. W.; van de Vijver, E.; Weterman, M. A. J.; de Boer, M.; Tool, A. T. J.; van den Berg, T. K.; Moser, M.; Jakobs, M. E.; Seeger, K.; Sanal, O.; Unal, S.; Cetin, M.; Roos, D.; Verhoeven, A. J.; Baas, F.
Date of Publication (YYYY-MM-DD): 2009-05-07
Title of Journal: Blood
Volume: 113
Issue / Number: 19
Start Page: 4740
End Page: 4746
Document Type: Article
ID: 431931.0
Leukocyte Adhesion Deficiency-1/variant syndrome is caused by mutations in FERMT3
Authors: van de Vijver, E.; Weterman, M. A.; de Boer, M.; Tool, A. T. J.; van den Berg, T. K.; Moser, M.; Jakobs, M. E.; Seeger, K.; Sanal, O.; Unal, S.; Roos, D.; Verhoeven, A. J.; Baas, F.; Kuijpers, T. W.
Date of Publication (YYYY-MM-DD): 2009-04
Title of Journal: European Journal of Clinical Investigation
Volume: 39
Issue / Number: Suppl. Suppl. 1
Start Page: 32
End Page: 32
Document Type: Article
ID: 423868.0
LAD-1/variant syndrome is caused by mutations in FERMT3
Authors: Kuijpers, T. W.; van de Vijver, E.; Weterman, M. A. J.; de Boer, M.; Tool, A. T. J.; van den Berg, T. K.; Moser, M.; Jakobs, M. E.; Seeger, K.; Sanal, O.; Unal, S.; Cetin, M.; Roos, D.; Verhoeven, A. J.; Baas, F.
Date of Publication (YYYY-MM-DD): 2008-12
Title of Journal: Blood
Start Page: o.Pag.
End Page: o.Pag.
Document Type: Article
ID: 408423.0
Entries: 1-4  
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