A Novel 12q13.2-q13.3 Microdeletion Syndrome With Combined Features of Diamond Blackfan Anemia, Pierre Robin Sequence and Klippel Feil Deformity

Overview of attention for article published in Frontiers in Genetics, November 2018

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RT @FrontGenetics: A novel 12q13.2-q13.3 microdeletion syndrome with combined features of Diamond Blackfan Anemia, Pierre Robin sequence an…

20 Nov 2018

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A novel 12q13.2-q13.3 microdeletion syndrome with combined features of Diamond Blackfan Anemia, Pierre Robin sequence and Klippel Feil deformity.: Domenico Roberti, Renata Conforti, Teresa Giugliano, Barbara Brogna, Immacolata Tartaglione, Maddalena… https

20 Nov 2018

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A novel 12q13.2-q13.3 #microdeletion #syndrome with combined features of #Diamond #Blackfan #Anemia , #Pierre #Robi..https://t.co/fC6YuHyCMP

19 Nov 2018

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