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- W2006235364 abstract "A 2-year-old boy with clinical manifestations of monosomy 9p syndrome and brown hair is described. G-banding and chromosome FISH studies demonstrated complex rearrangements involving seven breakpoints in chromosomes 2 and 9, which included a 6.6-Mb deletion at 9p22.2-p23. This, together with previous studies in the literature, narrowed the shortest region of overlap (SRO) for the syndrome to a 4.7-Mb interval. Candidate genes for trigonocephaly, mental retardation, and brown hair are discussed. © 2006 Wiley-Liss, Inc." @default.
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- W2006235364 date "2006-02-15" @default.
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- W2006235364 title "Narrowing candidate region for monosomy 9p syndrome to a 4.7-Mb segment at 9p22.2-p23" @default.
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- W2006235364 doi "https://doi.org/10.1002/ajmg.a.31094" @default.
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