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Human Mutation|October 6, 2011
Germline gain-of-function mutations of ALK disrupt central nervous system developmentLoïc de Pontual, Dania Kettaneh, Christopher T Gordon, et al.
The Journal of Pediatrics|September 18, 2010
Isolated congenital asplenia: a French nationwide retrospective survey of 20 casesNizar Mahlaoui, Veronique Minard-Colin, Capucine Picard, et al.
Annals of the Rheumatic Diseases|May 17, 2012
European registry of babies born to mothers with antiphospholipid syndromeArsene Mekinian, Eric Lachassinne, Pascale Nicaise-Roland, et al.
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