KA
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Title Published in Access level OA Policy Year Views Downloads
Diagnostic exome sequencing to elucidate the genetic basis of likely recessive disorders in consanguineous familiesHuman mutation
accessLevelRestricted
2014 697 4
De novo duplication of MECP2 in a girl with mental retardation and no obvious dysmorphic featuresClinical genetics
accessLevelRestricted
2010 682 0
L'apport de l'électrorétinographie multifocale dans le suivi des patients traités par hydroxychloroquine"
accessLevelPublic
2009 983 984
Intraocular lymphoma following a primary testicular lymphoma in remission for 10 yearsInternational ophtalmology
accessLevelPublic
2008 625 470
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