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Possible intrachromosomal duplication in a case of trisomy 9p
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Cytogenetic findings in 200 children with mental retardation and multiple congenital anomalies of unknown cause
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Duplication of the short arm of chromosome 9. Analysis of five cases
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Cuoco C, Gimelli G, Pasquali F, Poloni L, Zuffardi O, Alicata P, Battaglino G, Bernardi F, Cerone R, Cotellessa M, Ghidoni A, Motta S (1982): Duplication of the short arm of chromosome 9. Analysis of five cases. Hum Genet 61:3-7.
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Partial duplication of the short arm of chromosome 9(p13→p22) in a child with typical 9p trisomy phenotypc
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Non-mosaic tetrasomy 9p in a liveborn infant with multiple congenital anomalies: Case report and comparison with trisomy 9p
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Duplication 9p due to unequal sister chromatid exchange
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De novo tandem duplication 9p(p12→p24) with normal GALT activity in red cells
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Sur quatre cas de trisomie pour le bras court du chromosome 9. Individualisation d'une nouvelle entite morbide
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Evidence of structural heterogeneity from molecular cytogenetic analysis of dicentric Robertsonian translocation
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9p duplication confirmed by gene dosage effect. Report of two patients
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Zadeh TM, Funderburk SJ, Carrel R, Dumars KW (1981): 9p duplication confirmed by gene dosage effect. Report of two patients. Ann Genet 24:242-244.
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