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The patients revealed dysmorphic features and developmental delay with evident intrafamilial phenotypic variability. Mutual non robertsonian translocation is an uncommon event, and has not already been reported in patients with 22q11.2 deletions. The mechanism accountable for this uncommon form of translocation is discussed herein.Gentile F, Martino M, Santangelo L, Giordano P, Torres DD, Carbone V, Di Palma AM, Rossini M, Gesualdo L, Giordano P, Giordano M. From Uganda
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