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Halbertsma FJ, Neeleman C, Weemaes CM, et al. 
The absent and vanishing spleen: congenital asplenia and hyposplenism--two case reports. [Case Reports, Journal Article]
Acta Paediatr 2005 Mar; 94(3):369-71.
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Gilbert B, Menetrey C, Belin V, et al. 
Familial isolated congenital asplenia: a rare, frequently hereditary dominant condition, often detected too late as a cause of overwhelming pneumococcal sepsis. Report of a new case and review of 31 others. [Case Reports, Journal Article, Review]
Eur J Pediatr 2002 Jul; 161(7):368-72.
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Nagel BH, Williams H, Stewart L, et al. 
Splenic state in surviving patients with visceral heterotaxy. [Comment, Journal Article]
Cardiol Young 2005 Oct; 15(5):469-73.
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Kanthan R, Moyana T, Nyssen J 
Asplenia as a cause of sudden unexpected death in childhood. [Case Reports, Journal Article]
Am J Forensic Med Pathol 1999 Mar; 20(1):57-9.
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Katcher AL 
Familial asplenia, other malformations, and sudden death. [Case Reports, Journal Article]
Pediatrics 1980 Mar; 65(3):633-5.
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Germing U, Perings C, Steiner S, et al. 
Congenital asplenia detected in a 60 year old patient with septicemia. [Case Reports, Journal Article]
Eur J Med Res 1999 Jul 28; 4(7):283-5.
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Beytout J, Tournilhac O, Laurichesse H 
[Asplenia and hyposplenism] [Journal Article]
Presse Med 2003 Sep 6; 32(28 Suppl):S5-9.
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Wagman PG, Dworkin HJ 
Splenic imaging in a patient with functional asplenia. [Case Reports, Journal Article]
Clin Nucl Med 1989 Apr; 14(4):264-7.
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Corazza GR, Ginaldi L, Zoli G, et al. 
Howell-Jolly body counting as a measure of splenic function. A reassessment. [Journal Article]
Clin Lab Haematol 1990; 12(3):269-75.
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