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Duplication of the short arm of chromosome 9: Analysis of five cases
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0017232219
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Centric fission of chromosome No4 in the mother of two patients with trisomy 4p
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47, +(9q-) in unrelated three children with plasma growth hormone deficiency
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0020595173
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Trisomie du bras court du 9 avec isochromosome 9p et monosomie partielle Yq
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0018289516
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Trisomy 9p with i(9p) and t(9q18p)
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Complete trisomy 5p de novo translocation t(2;5)(q36;p11) with isochromosome 5p: Case report and review of the literature
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Leschot NJ, Lim KS (1979): Complete trisomy 5p de novo translocation t(2;5)(q36;p11) with isochromosome 5p: Case report and review of the literature. Hum Genet 46:271-278.
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Chromosome 9, trisomy 9
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Complete trisomy 5p owing to de novo translocation t(5;22)(q11;p11) with isochromosome 5p associated with a familial pericentric inversion of chromosome 2, inv 2 (p21;q11)
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Orye E, Benoit Y, Van Mele B (1983): Complete trisomy 5p owing to de novo translocation t(5;22)(q11;p11) with isochromosome 5p associated with a familial pericentric inversion of chromosome 2, inv 2 (p21;q11). J Med Genet 20:394-396.
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Trisomy for the short arms of chromosome 9 in two generations, with balanced traslocations t(15p+;9q-) in three generations
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Centric fission, centromere-telomere fusion and isochromosome formation: A possible origin of a de novo 12p trisomy
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A human chromosome 9-specific alphoid DNA repeat specially resolvable from satellite 3 DNA by fluorescence in situ hybridization
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Types, stability, and phenotypic consequences of chromosome rearrangements leading to interstitial telomeric sequences
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Rossi E, Floridia G, Casali M, Danesino C, Chiumello G, Bernardi F, Magnani I, Papi L, Mura M, Zuffardi O (1993): Types, stability, and phenotypic consequences of chromosome rearrangements leading to interstitial telomeric sequences. J Med Genet 30:926-931.
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Trisomy 9p resulting from de novo 9/15 translocation and a 9p isochromosome
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