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Scapula alata as presenting symptom of Fanconi anemia: A case for serendipity.
Clin Case Rep. 2019 Jul 23;7(9):1660-1662. doi: 10.1002/ccr3.2323. eCollection 2019 Sep.
Clin Case Rep. 2019.
PMID: 31534721
Free PMC article.
Deletion of the 3q26 region including the EVI1 and MDS1 genes in a neonate with congenital thrombocytopenia and subsequent aplastic anaemia.
Nielsen M, Vermont CL, Aten E, Ruivenkamp CA, van Herrewegen F, Santen GW, Breuning MH.
Nielsen M, et al. Among authors: van herrewegen f.
J Med Genet. 2012 Sep;49(9):598-600. doi: 10.1136/jmedgenet-2012-100990.
J Med Genet. 2012.
PMID: 22972950
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Clinical practice: the bleeding child. Part II: disorders of secondary hemostasis and fibrinolysis.
van Herrewegen F, Meijers JC, Peters M, van Ommen CH.
van Herrewegen F, et al.
Eur J Pediatr. 2012 Feb;171(2):207-14. doi: 10.1007/s00431-011-1571-x. Epub 2011 Sep 17.
Eur J Pediatr. 2012.
PMID: 21922352
Free PMC article.
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