References
Abe, T., Morita, M. P., Kawai, K., Misawa, S., Takino, T., Hashimoto, H., Nakagome, Y.: Partial tetrasomy 9 (9qter→9q2101) due to an extra isodicentric chromosome. Ann. Genet. (Paris) 20, 111–114 (1977)
Ferguson-Smith, M. A.: Human cytogenetics. In: Birth defects, J. W. Littlefield, J. de Grouchy (eds.), pp. 349–357. Amsterdam: Excerpta Medica 1978
Fujita, H., Shimazaki, M., Takeuchi, T., Hayakawa, Y., Oura, T.: 47,+(9q-) in unrelated three children with plasma growth hormone deficiency. Hum. Genet. 31, 271–282 (1976)
Ghymers, D., Hermann, B., Disteche, C., Frederic, J.: Tetrasomie partielle du chromosome 9, a l'etat de mosaique chez un enfant porteur de malformations multiples. Hum. Genet. 20, 273–282 (1973)
Gripenberg, U., Hongell, K., Iivanainen, M., Kivimaki, T.: Free trisomy 9p in an elderly woman. Ann. Genet. (Paris) 20, 36–40 (1977)
Grouchy, J. de, Turleau, C.: Clincal atlas of human chromosomes, p. 75. New York: Wiley 1977
Hoehn, H., Engel, W., Reinwein, H.: Presumed trisomy for the short arm of 9 not due to inherited translocation. Humangenetik 12, 175–181 (1971)
Kaijser, K.: Case report of an extra, small, acrocentric chromosome in a non-mongoloid girl. Clin. Genet. 5, 254–258 (1974)
Kaosaar, M. E., Mikelsaar, A. V. N., Talvik, T. A., Mikelsaar, R. V. A.: A case of trisomy for the short arm of chromosome no. 9 (+9p). Hum. Genet. 34, 77–80 (1976)
Kardon, N. B., Salwen, H. R., Krauss, M. A., Davis, J. G., Jenkins, E. C. De novo trisomy 9pter→q13. Hum. Genet. 37, 149–153 (1977)
Lin, C. C., Holman, G., Sewell, G., Bowen, P., Biederman, B.: Interchromosomal duplication for the short arm of chromosome no. 9: Report of three cases due to a familial translocation t(9;11) and one case with a de novo 47,XX,+9p karyotype. J. Ment. Defic. Res. 21, 309–329 (1977)
Orye, E., Verhaaren, H., Van Egmond, H., Devloo-Blancquaert, A.: A new case of the trisomy 9p syndrome. Report of a patient with unusual chromosome findings (46,XX/47,XX,+i(9p)) and a peculiar congenital heart defect. Clin. Genet. 7, 134–143 (1975)
Rutten, F. J., Scheres, J. M. J. C., Hustinx Th. W. J., der Haar, B. G. A.: A presumptive tetrasomy for the short arm of chromosome 9. Hum. Genet. 25, 163–170 (1974)
Smith, G., McCaa, A., Kelly, T. E.: Trisomy 9p with an isochromosome of 9p. Hum. Genet. 42, 93–97 (1978)
Turleau, C., de Grouchy, J., Roubin, M., Chavin-Colin, F., Cachin, O.: Trisomy 9p pure 47,XX,+de(9)(q11). Découverte d'un cellule 46,XY,del(9)(q11) chez le pere. Ann. Genet. (Paris) 18, 125–129 (1975)
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Biederman, B. Trisomy 9p with an isochromosome of 9p. Hum Genet 46, 125–126 (1979). https://doi.org/10.1007/BF00278912
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DOI: https://doi.org/10.1007/BF00278912