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References
Asano T, Ikeuchi T, Shinohara T, Enokido H, ashimoto K. Partial 18q trisomy and 18p monosomy resulting from a maternal pericentric inversion, (Review).Jap J Hum Genet 1991; 36 (3): 257–265.
Fried K, Bar-Yochal A, Rosenblatt M, Mundel G. Partial 18 trisomy (with 47 chromosomes) resulting from a familial maternal translocation.J Med Genet 1978; 15: 76–78.
Fryns JP, Detavernier F, Van Fleteren A, Van den Berghe H. Partial trisomy 18q in a newborn with typical 18 trisomy phenotype.Hum Genet 1978; 44: 201–205.
Fryns JP, Vinken L, Merien J, Van den Berghe H. Partial trisomy 18q12, due to intrachromosomal duplication, is not associated with typical 18 trisomy phenotype.Hum Genet 1979; 46: 341–344.
Matsuoka R, Matsuyama S, Yamamoto Yet al. Trisomy 18q. A case report and review of karyotype-phenotype correlations.Hum Genet 1981; 57: 78–82.
Mewar R, Kline AD, Harrison Wet al. Clinical and molecular evaluation of four patients with partial duplications of the long arm of chromosome 18. (Review).Am J Hum Genet 1993; 53 (6): 1269–1278.
Neu RL, Ortega CC, Barg GAet al. Inclusion of satellites in a 18/21 translocation chromosome shown by ammoniacal-silver staining (sat-banding) in case of partial trisomy 18.J Med Genet 1976; 13: 520–522.
Pluchon E, Giovangrandi Y, Labbe Fet al. Prenatal diagnosis of a fetus with partial monosomy 7(q34 qter)and partial trisomy 18(q21 qter).Prenat Diagn 1993; 13 (10): 983–988.
Turleau C, Grouchy J de. Trisomy 18qter and trisomy mapping of chromosome 18.Clin Genet 1977; 12: 361–371.
Wilson GN, Heller KB, Elterman RD, Schneider NR. Partial trisomy 18 with minimal anomalies: Lack of corresondence between phenotypic manifestations and triplicated loci along chromosome 18. (Review).Am J Med Genet 1990; 36 (4): 506–510.
Vivarelli R, Paolieri M, Anichini Cet al. Correlations between karyotype and phenotype in structural and numerical abnormalities of chromosome 18.Bull soc Ital Biol Sper 1992; 68 (4): 263–269.
Wolf DJ, Schwartz MF, Cohen MM, Schwartz S. Precise mapping of a de novo duplication 18 (q21 q22) utilizing cytogenetic, biochemical and molecular techniques.Am J Med Genet 1993; 46 (5): 520–523.
Moorhead PS, Nowell PC, Mellman WJet al. Chromosome preparations of leucocytes cultured from peripheral blood.Exp Cell Res 1960; 613–616.
Verma RS, Babu A.Human Chromosomes: Manual of Basic Techniques. New York: Pergamon Press, 1989; 45–114.
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Elbistan, M., Kucukoduk, S. & Kara, N. Partial trisomy 18q. Indian J Pediatr 63, 393–396 (1996). https://doi.org/10.1007/BF02751537
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DOI: https://doi.org/10.1007/BF02751537