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bibliographicCitation Siggberg L, Peippo M, Sipponen M, Miikkulainen T, Shimojima K, Yamamoto T, Ignatius J, Knuutila S. 9q22 Deletion - First Familial Case. Orphanet Journal of Rare Diseases. 2011 Jun 22;6(1):45. doi: 10.1186/1750-1172-6-45.
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title 9q22 Deletion - First Familial Case
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