A third case of de novo partial trisomy 4 pOORTHUYS, J. W. E; GERSSEN-SCHOORL, K. B. J; DE PATER, J. M et al.Journal of medical genetics. 1989, Vol 26, Num 5, pp 344-345, issn 0022-2593, 2 p.Article

De novo partial trisomy 15q (proximal type)HERWEIJER, T. J; OORTHUYS, J. W. E; LESCHOT, N. J et al.Journal of medical genetics. 1988, Vol 25, Num 4, pp 260-262, issn 0022-2593Article

A new case of partial 2p trisomy due to de novo interstitial duplication 2p21-22PARRUTI, G; DI ILIO, C; CALABRESE, G et al.Annales de génétique (Paris). 1989, Vol 32, Num 1, pp 55-58, issn 0003-3995, 4 p.Article

Partial trisomy 9 ― further delineation of the phenotypeSMART, R. D; VILJOEN, D. L; FRASER, B et al.American journal of medical genetics. 1988, Vol 31, Num 6, pp 947-951, issn 0148-7299Article

Distal trisomy 14qMIKELSAAR, R. V.-A; ILUS, T. A; LURIE, I. W et al.Journal of medical genetics. 1987, Vol 24, Num 6, pp 380-381, issn 0022-2593Article

Partial Trisomy 4q Associated With Young-Onset Dopa-Responsive ParkinsonismGARRAUX, Gaetan; CABERG, Jean-Hubert; VANBELLINGHEN, Jean-François et al.Archives of neurology (Chicago). 2012, Vol 69, Num 3, pp 398-400, issn 0003-9942, 3 p.Article

Partial Chromosome Deletion: A New Trisomy Rescue Mechanism?VIALARD, F; MOLINA-GOMES, D; QUARELLO, E et al.Fetal diagnosis and therapy. 2009, Vol 25, Num 1, pp 111-114, issn 1015-3837, 4 p.Article

Trisomy 1q42→qter in a sister and brother : further delineation of the trisomy 1q42→qter syndromeVERSCHUUREN-BEMELMANS, C. C; LEEGTE, B; HODENIUS, T. M. J et al.American journal of medical genetics. 1995, Vol 58, Num 1, pp 83-86, issn 0148-7299Article

Trisomy 1q in a case of essential thrombocythemia with long survivalRICHARD, C; CONDE, E; GARIJO, J et al.Cancer genetics and cytogenetics. 1987, Vol 25, Num 1, pp 185-186, issn 0165-4608Article

Further delineation of the partial proximal trisomy 10q syndromeAALFS, C. M; HOOVERS, J. M. N; NIESTE-OTTER, M. A et al.Journal of medical genetics. 1995, Vol 32, Num 12, pp 968-971, issn 0022-2593Article

Partial trisomy chromosome 5 cosegregating with schizophreniaBASSETT, A. S; MCGILLIVRAY, B. C; JONES, B. D et al.Lancet (British edition). 1988, Num 8589, pp 799-801, issn 0140-6736Article

Trisomy (1q) (q42→qter): confirmation of a syndromeCHIA, N. L; BOUSFIELD, L. R; POON, C. C. S et al.Clinical genetics. 1988, Vol 34, Num 4, pp 224-229, issn 0009-9163Article

Partial mosaic trisomy 5: A new case report with ocular involvementSCHLEGEL, Z; VALENT, A; HIRSCH, A et al.Journal français d'ophtalmologie. 2009, Vol 32, Num 8, pp 553-559, issn 0181-5512, 7 p.Article

Two siblings with partial trisomy 1(q42.3-ter)SUNAGA, Y; OHTSUKA, T; NAGASHIMA, K et al.Brain & development (Tokyo. 1979). 1993, Vol 15, Num 2, pp 119-124, issn 0387-7604Article

Partial trisomies in two spontaneously arising long-lived human keratinocyte linesDONALD WEAVER, J; STETTEN, G; LITTLEFIELD, J. W et al.In vitro cellular & developmental biology. 1991, Vol 27A, Num 8, pp 670-675, issn 0883-8364Article

Partial trisomy 18 with minimal anomalies : lack of correspondence between phenotypic manifestations and triplicated loci along chromosome 18WILSON, G. N; HELLER, K. B; ELTERMAN, R. D et al.American journal of medical genetics. 1990, Vol 36, Num 4, pp 506-510, issn 0148-7299Article

Brief clinical report: phenotype-karyotype correlations in dup (18q): report of a case and reviewRAZAVI-ENCHA, F; RAOUL, O; LESCS, M.-C et al.American journal of medical genetics. 1985, Vol 21, Num 3, pp 591-595, issn 0148-7299Article

Partial trisomy 7 (q32→qter) syndrome in two childrenCOUZIN, D. A; HAITES, N; WATT, J. L et al.Journal of medical genetics. 1986, Vol 23, Num 5, pp 461-465, issn 0022-2593Article

Clinical, chromosomal and enzymatic studies in four cases of rearrangements of chromosome 7BAETEMAN, M. A; PHILIP, N; MATTEI, M. G et al.Clinical genetics. 1985, Vol 27, Num 6, pp 564-569, issn 0009-9163Article

Case report: partial trisomy 20q (20q13.13→qter)SAX, C. M; BODURTHA, J. N; BROWN, J. A et al.Clinical genetics. 1986, Vol 30, Num 6, pp 462-465, issn 0009-9163Article

Craniosynostosis with extra copy of MSX2 in a patient with partial 5q-trisomySHIIHARA, Takashi; KATO, Mitsuhiro; KIMURA, Toshiyuki et al.American journal of medical genetics. 2004, Vol 128A, Num 2, pp 214-216, issn 0148-7299, 3 p.Article

Prenatal diagnosis of 47,XX, der(15)t(15;16)(q13;p13.2)SANTOLAYA-FORGAS, Joaquin; DE LEON, Juan; POWELL, Wm. Cameron et al.Prenatal diagnosis. 2004, Vol 24, Num 3, pp 209-212, issn 0197-3851, 4 p.Article

Partial 15q22 trisomy due to segregation of maternal 10;15 reciprocal translocationPRABHAKARA, K; DUTTA, Usha; RADHA RAMADEVI, A et al.Indian pediatrics. 2002, Vol 39, Num 11, pp 1050-1054, issn 0019-6061, 5 p.Article

Pre- and perinatal findings in partial trisomy 7q resulting from balanced parental translocations t(7;21) and t(4;7)COURTENS, W; VROMAN, S; VANDENHOVE, J et al.Prenatal diagnosis. 2001, Vol 21, Num 8, pp 642-648, issn 0197-3851Article

Pure trisomy lop resulting from an extra ring chromosome: Characterization by methods of advanced molecular cytogeneticsZHONG CHEN; MELONI-EHRIG, Aurelia; PALUMBOS, Janice C et al.American journal of medical genetics. 2001, Vol 102, Num 4, pp 379-382, issn 0148-7299Article