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0017759883
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New chromosomal dysmorphic syndromes. 2. Trisomy 10p
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Stengel-Rutkowski, S.1
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Riechert, M.4
Spiess, H.5
Rodewald, A.6
Stene, J.7
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2
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0029854179
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Trisomy 10p. Report of an unusual mechanism of formation and critical evaluation of the clinical phenotype
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Clement SJ, Leppig KA, Jarvik GP, Kapur RP, Norwood TH. Trisomy 10p. Report of an unusual mechanism of formation and critical evaluation of the clinical phenotype. Am J Med Genet 1996: 65: 197-204.
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Clement, S.J.1
Leppig, K.A.2
Jarvik, G.P.3
Kapur, R.P.4
Norwood, T.H.5
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4
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0026516889
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Isochromosome duplication of 10p and translocation of 10q
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Rivera H, Rivas F. Isochromosome duplication of 10p and translocation of 10q. Am J Med Genet 1992: 42: 396-397.
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Rivera, H.1
Rivas, F.2
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5
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0021240891
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A de novo case of trisomy 10p: Gene dosage studies of hexokinase, inorganic pyrophosphatase and adenosine kinase
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Snyder FF, Lin CC, Rudd NL, Shearer JE, Heikkila EM, Hoo JJ. A de novo case of trisomy 10p: gene dosage studies of hexokinase, inorganic pyrophosphatase and adenosine kinase. Hum Genet 1984: 67: 187-189.
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Snyder, F.F.1
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Rudd, N.L.3
Shearer, J.E.4
Heikkila, E.M.5
Hoo, J.J.6
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6
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0021202479
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Duplication of chromosome 10p: Confirmation of regional assignments of platelet-type phosphofructokinase
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Schwartz S, Cohen MM, Panny SR, Beisel JH, Vora S. Duplication of chromosome 10p: confirmation of regional assignments of platelet-type phosphofructokinase. Am J Hum Genet 1984: 36: 750-759.
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Schwartz, S.1
Cohen, M.M.2
Panny, S.R.3
Beisel, J.H.4
Vora, S.5
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7
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0018429347
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Trisomy 10p due to a de novo t(10p;13p)
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Aller V, Abrisqueta JA, Perez-Castillo A, del Mazo J, Martin-Lucas MA, de Torres ML. Trisomy 10p due to a de novo t(10p;13p). Hum Genet 1979: 46: 129-134.
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Aller, V.1
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De Torres, M.L.6
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8
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0029788688
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Breakpoint diversity illustrates distinct mechanisms for Robertsonian translocation formation
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Page SL, Shin J-C, Han J-Y, Choo KHA, Shaffer LG. Breakpoint diversity illustrates distinct mechanisms for Robertsonian translocation formation. Hum Mol Genet 1996: 5: 1279-1288.
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Page, S.L.1
Shin, J.-C.2
Han, J.-Y.3
Choo, K.H.A.4
Shaffer, L.G.5
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9
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0031441043
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Early urethral obstruction sequence and unbalanced translocation with terminal 10p duplication/1p deficiency
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Fryns JP, Vandenberghe K, Deschrijver D. Early urethral obstruction sequence and unbalanced translocation with terminal 10p duplication/1p deficiency. Genet Couns 1997: 8: 349-350.
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Fryns, J.P.1
Vandenberghe, K.2
Deschrijver, D.3
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10
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0029814318
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Characterization of familial partial 10p trisomy by chromosomal microdissection, FISH, and microsatellite dosage analysis
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Stone D, Ning Y, Guan XY, Kaiser-Kupfer M, Wynshaw-Boris A, Biesecker L. Characterization of familial partial 10p trisomy by chromosomal microdissection, FISH, and microsatellite dosage analysis. Hum Genet 1996: 98: 396-402.
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Stone, D.1
Ning, Y.2
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Kaiser-Kupfer, M.4
Wynshaw-Boris, A.5
Biesecker, L.6
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11
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0028147096
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10p duplication characterized by fluorescence in situ hybridization
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Wiktor A, Feldman GL, Kratkoczki P. Ditmars DMJr, Van Dyke DL. 10p duplication characterized by fluorescence in situ hybridization. Am J Med Genet 1994: 52: 315-318.
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Wiktor, A.1
Feldman, G.L.2
Kratkoczki, P.3
Ditmars D.M., Jr.4
Van Dyke, D.L.5
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12
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0028904945
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Family with partial monosomy 10p and trisomy 10p
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Hon E, Chapman C, Gunn TR. Family with partial monosomy 10p and trisomy 10p. Am J Med Genet 1995: 56: 136-140.
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Hon, E.1
Chapman, C.2
Gunn, T.R.3
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13
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0021153464
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Trisomy for the short arm of chromosome 10: Report of a new case resulting from segregation of a maternal balanced translocation t(10qter-q11::14q11-qter)
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Delaroche I, Bruni L, Giannotti A, Giampaolo R, Aebischer ML. Trisomy for the short arm of chromosome 10: report of a new case resulting from segregation of a maternal balanced translocation t(10qter-q11::14q11-qter). Helv Paediat Acta 1984: 39: 161-166.
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Delaroche, I.1
Bruni, L.2
Giannotti, A.3
Giampaolo, R.4
Aebischer, M.L.5
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14
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0028137843
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Familial 10p trisomy resulting from a maternal pericentric inversion
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Kozma C, Meek JM. Familial 10p trisomy resulting from a maternal pericentric inversion. Am J Med Genet 1994: 49: 281-287.
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Kozma, C.1
Meek, J.M.2
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16
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0017082813
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Trisomie 4p de novo par isochromosome 4p
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Andre MJ, Aurias A, Berranger P, Gillot F, Lefranc G, Lejeune J. Trisomie 4p de novo par isochromosome 4p. Ann Genet Paris 1976: 19: 127-131.
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Andre, M.J.1
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Gillot, F.4
Lefranc, G.5
Lejeune, J.6
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17
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0018734363
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'Complete' trisomy 5p: De novo translocation t(2;5)(q36:P11) with isochromosome 5p. Case report and review of literature
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Leschot NJ, Lim KS. 'Complete' trisomy 5p: de novo translocation t(2;5)(q36:p11) with isochromosome 5p. Case report and review of literature. Hum Genet 1979: 46: 271-278.
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Leschot, N.J.1
Lim, K.S.2
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18
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0020506651
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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. 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 1983: 20: 394-396.
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Orye, E.1
Benoit, Y.2
Van Mele, B.3
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19
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0028234224
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A new case of 'complete' trisomy 5p with isochromosome 5p associated with a de novo translocation t(5;8)(q11;p23)
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Fujita M, Flori E. Lemaire F, Casanova R, Astruc D. A new case of 'complete' trisomy 5p with isochromosome 5p associated with a de novo translocation t(5;8)(q11;p23). Clin Genet 1994: 45: 305-307.
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Fujita, M.1
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Casanova, R.4
Astruc, D.5
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20
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0017814360
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Trisomy 9p with an isochromosome of 9p
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Smith G, McCaa A, Kelly TE. Trisomy 9p with an isochromosome of 9p. Hum Genet 1978: 42: 93-97.
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Smith, G.1
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21
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0018289516
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Trisomy 9p with i(9p) and t(9q;18p)
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Herva R, Koivisto M. Trisomy 9p with i(9p) and t(9q;18p). Hum Genet 1979: 509: 237-240.
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Hum Genet
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Herva, R.1
Koivisto, M.2
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22
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0018644882
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Trisomy 9p resulting from de novo 9/15 translocation and a 9p isochromosome
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Sandig KR, Mucke J. Veit H. Trisomy 9p resulting from de novo 9/15 translocation and a 9p isochromosome. Hum Genet 1979: 52: 175-178.
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Sandig, K.R.1
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23
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0023192019
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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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Rivera H, Garcia-Esquivel L, Jimenez-Sainz M, Vaca G, Ibarra B, Cantu JM. Centric fission, centromere-telomere fusion and isochromosome formation: a possible origin of a de novo 12p trisomy. Clin Genet 1987: 31: 393-398.
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Rivera, H.1
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Jimenez-Sainz, M.3
Vaca, G.4
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Cantu, J.M.6
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24
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0024347093
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A case of de novo i(12p) with 12q whole-arm translocation mosaicism
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Marques-de-Faria AP, Hackel C. A case of de novo i(12p) with 12q whole-arm translocation mosaicism. Am J Med Genet 1989: 32: 453-456.
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Marques-De-Faria, A.P.1
Hackel, C.2
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25
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0021989863
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Trisomy 10p, due to an unusual translocation
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Orye E, Van Haesebrouck P, Van Coster R, Van Mele B. Trisomy 10p, due to an unusual translocation. J Genet Hum 1985: 33: 63-66.
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J Genet Hum
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Orye, E.1
Van Haesebrouck, P.2
Van Coster, R.3
Van Mele, B.4
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