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0034706403
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Distal 5q trisomy resulting from an X;5 translocation detected by chromosome painting
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2
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4644289236
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Familial insertion (3;5)(q25.3; q22.1q31.3) with deletion or duplication of chromosome region 5q22.1-5q31.3 in ten unbalanced carriers
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Arens YH, Engelen JJ, Govaerts LC, et al. 2004. Familial insertion (3;5)(q25.3; q22.1q31.3) with deletion or duplication of chromosome region 5q22.1-5q31.3 in ten unbalanced carriers. Am J Med Genet A 130:128-133.
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3
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14644433671
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Recombination aneusomy of subtelomeric regions of chromosome 5, resulting from a large familial pericentric inversion inv(5)(p15.33q35.3)
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Bocian E, Suchenek K, Obersztyn E, et al. 2005. Recombination aneusomy of subtelomeric regions of chromosome 5, resulting from a large familial pericentric inversion inv(5)(p15.33q35.3). J Appl Genet 46:109-114.
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4
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0027440264
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Paternal duplication of chromosome 5q11.2-5q14 in a male born with craniostenosis, ear tags, kidney dysplasia and several other anomalies
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Breslau-Siderius EJ, Wijnen JTh, Dauwerse JG, et al. 1993. Paternal duplication of chromosome 5q11.2-5q14 in a male born with craniostenosis, ear tags, kidney dysplasia and several other anomalies. Hum Genet 92:481-485.
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5
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0021680510
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Balanced rearrangement of chromosomes 2,5, and 13 in a family with duplication 5q and fetal loss
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Evans MI, White BJ, Kent SG, et al. 1984. Balanced rearrangement of chromosomes 2,5, and 13 in a family with duplication 5q and fetal loss. Am J Med Genet 19:783-790.
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Evans, M.I.1
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6
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0023618112
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Distinct dysmorphic syndrome in a child with inverted distal 5q duplication
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7
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0019868056
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Partial proximal trisomy of the long arm of chromosome 5 (q13-q22) resulting from maternal insertion der ins (10;5)
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Gilgenkrantz S, Dulucq P, Bresson JL, et al. 1981. Partial proximal trisomy of the long arm of chromosome 5 (q13-q22) resulting from maternal insertion der ins (10;5). J Med Genet 18:465-480.
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Gilgenkrantz, S.1
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8
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0016779785
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Partial trisomy for the long arms of chromosome no. 5 due to insertion and further 'aneusomie de recombinaison'
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Jalbert P, Jalbert H, Sele B, et al. 1975. Partial trisomy for the long arms of chromosome no. 5 due to insertion and further 'aneusomie de recombinaison'. J Med Genet 12:418-423.
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Jalbert, P.1
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9
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0018572187
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Tandem duplication (5q13-22) in a mentally deficient girl
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Kessel E, Pfeiffer RA. 1979. Tandem duplication (5q13-22) in a mentally deficient girl. Hum Genet 52:217-220.
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10
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0023134292
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Clinical manifestations of trisomy 5q
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Kumar D, Heath PR, Blank CE. 1987. Clinical manifestations of trisomy 5q. J Med Genet 24:180-184.
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Kumar, D.1
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11
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0026708985
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Simultaneous partial monosomy 10p and trisomy 5q in a case of hypoparathyroidism
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Lai MM, Scriven PN, Ball C, Berry AC. 1992. Simultaneous partial monosomy 10p and trisomy 5q in a case of hypoparathyroidism. J Med Genet 29: 586-588.
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Lai, M.M.1
Scriven, P.N.2
Ball, C.3
Berry, A.C.4
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12
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0037085682
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Delineation of the dup 5q phenotype by molecular cytogenetic analysis in a patient with dup5q/del 5p (cri du chat)
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Levy B, Dunn TM, Kern JH, et al. 2002. Delineation of the dup 5q phenotype by molecular cytogenetic analysis in a patient with dup5q/del 5p (cri du chat). Am J Med Genet 108:192-197.
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Levy, B.1
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13
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0031963879
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Familial dup(5)(q15q21) associated with normal and abnormal phenotypes
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Li SY, Gibson LH, Gomez K, et al. 1998. Familial dup(5)(q15q21) associated with normal and abnormal phenotypes. Am J Med Genet 75:75-77.
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Li, S.Y.1
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14
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0033597185
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Duplication within chromosome 5q characterized by fluorescence in situ hybridization
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Mowat D, Jauch A, Robson L, Smith A. 1999. Duplication within chromosome 5q characterized by fluorescence in situ hybridization. Am J Med Genet 83:361-364.
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Mowat, D.1
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15
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0020057636
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Fetal manifestation of a chromosomal disorder: Partial duplication of the long arm of chromosome 5 (5q33 to qter)
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Passarge E, Bartsch-Sandhoff M, Rehder H. 1982. Fetal manifestation of a chromosomal disorder: partial duplication of the long arm of chromosome 5 (5q33 to qter). Teratology 25:221-225.
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Passarge, E.1
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16
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0018911307
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Partial trisomie 5q: Three different phenotypes depending on different duplication segments
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Rodewald A, Zankl M, Gley EO, Zang KD. 1980. Partial trisomie 5q: three different phenotypes depending on different duplication segments. Hum Genet 55:191-198.
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Rodewald, A.1
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Zang, K.D.4
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18
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0034521043
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Cryptic translocation t(5;18) in familial mental retardation
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Vogels A, Devriendt K, Verrneesch JR, et al. 2000. Cryptic translocation t(5;18) in familial mental retardation. Ann Genet 43:117-123.
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Vogels, A.1
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19
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0024392548
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Duplication of 5q11.2-q13.1 from a familial (5;20) balanced insertion
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Yip MY, Kemp J, Hanson N, et al. 1989. Duplication of 5q11.2-q13.1 from a familial (5;20) balanced insertion. Am J Med Genet 32:220-223.
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Yip, M.Y.1
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