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In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
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HDR syndrome: a novel "de novo" mutation in GATA3 gene

Silvio Ferraris1, Angelo Giovanni Del Monaco, Emanuela Garelli

  • 1Department of Pediatrics, University of Torino, Torino, Italy. silvio.ferraris@unito.it

American Journal of Medical Genetics. Part A
|February 28, 2009
PubMed

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