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A child with bisatellited, dicentric chromosome 15 arising from a maternal paracentric inversion of chromosome 15q.
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2
[Severe mental retardation and slight dysmorphism in a child with a bisatellite extrachromosome: inversion duplication (15)?].
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A familial paracentric inv(1)(q42q44) resulting in a child with a del(1)(q42) karyotype.
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Pericentric inversion of chromosome "20" associated with congenital anomalies.
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Duplication of medial 15q confirmed by FISH.
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Recombinant chromosome 9 possibly derived from breakage and reunion of sister chromatids within a paracentric inversion loop.
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Partial tetrasomy 15 due to a unique inverted triplication of chromosome15q24-q26.
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Inv dup(15) supernumerary marker chromosomes.
J Med Genet. 1994 Aug;31(8):585-94. doi: 10.1136/jmg.31.8.585.
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Interstitial 3p deletion in a child due to paternal paracentric inserted inversion.
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Large inv dup(15) chromosome in two generations.
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Disruption of chromodomain helicase DNA binding protein 2 (CHD2) causes scoliosis.
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Array based characterization of a terminal deletion involving chromosome subband 15q26.2: an emerging syndrome associated with growth retardation, cardiac defects and developmental delay.
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