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Vici syndrome
Orphanet Report Series Rare Diseases Collection
Mackenzie's Mission Gene & Condition List
Mackenzie's Mission Gene & Condition List
Whole Exome Sequencing Gene Package Intellectual Disability, Version 9.1, 31-1-2020
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Case Report Vici Syndrome: a Rare Autosomal Recessive Syndrome with Brain Anomalies, Cardiomyopathy, and Severe Intellectual Disability
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ORPHA Number Disease Or Group of Diseases 300305 11P15.4
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Orphanet Report Series 180 160 Collection 140 Rare Diseases
WO 2016/069591 A2 6 May 2016 (06.05.2016) W P O P C T
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Prevalence and Incidence of Rare Diseases: Bibilographic Data
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Vici Syndrome
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Vici Syndrome in an Egyptian Infant: Case Report and Differential
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Vici Syndrome: a Review Susan Byrne1, Carlo Dionisi-Vici2, Luke Smith3, Mathias Gautel3 and Heinz Jungbluth1,3,4*
Orphanet Report Series 180 160 Collection 140 Rare Diseases
Prevalence and Incidence of Rare Diseases
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Orphanet Report Series 180 160 Collection 140 Rare Diseases
Prevalence and Incidence of Rare Diseases: Bibliographic Data
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Orphanet Report Series Rare Diseases Collection
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Nuove Politiche Per L'innovazione Nel Settore Delle Scienze Della Vita