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De novo tandem duplication of chromosome segment 22q11-q12: Clinical, cytogenetic, and molecular characterization
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Assignment of the gene encoding the human thyrotropin-releasing hormone receptor to 8q23 by fluorescence in situ hybridization
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Isolation and mapping of 328 new cosmid markers on human chromosome 8: Construction of a high-resolution cytogenetic map of chromosome 8 with 416 markers
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Partial trisomy of distal 8q derived from mother with mosaic 8q23.3-24.13 deletion, and relatively mild expression of trichorhinophalangeal syndrome I
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CHARGE association in a child with de novo inverted duplication (14)(q22-q24.3)
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The origin of cytologically unidentifiable chromosome abnormalities: Six cases ascertained by targeted chromosome-band painting
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Partial trisomy 13q identified by sequential fluorescence in situ hybridization
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Interstitial duplication 19p
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Partial duplication 8q12-q21.2 in two sibs with maternally derived insertional and reciprocal translocations: Case reports and review of partial duplications of chromosome 8
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De novo nonreciprocal translocation 1;8 confirmed by fluorescent in situ hybridization
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19
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Patient with de novo 12p+ syndrome identified as dir dup(12)(p13) using subchromosomal painting libraries from somatic cell hybrids
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Further contribution to the description of phenotypes associated with partial 4q duplication
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