Log in or create a free account to read this content
Gain free access to this article, as well as selected content from this journal and more on nature.com
or
References
Allderdice, P.W., Eales, B., Onyett, H., Sprague, W., Henderson, K., Lefeuvre, P.A., and Pal, G. 1983. Duplication 9q34 syndrome.Am. J. Hum. Genet. 35: 1005–1019.
Cohen, M.M., Lerner, C., and Balkin, N.E. 1983. Duplication of 16p from insertion of 16p into 16q with subsequent duplication due to crossing over within the inserted segment.Am. J. Med. Genet. 14: 89–96.
Grass, F.S., Schwartz, R.P., Deal, J.O., and Parke, J.C. 1981. Gonadal dysgenesis, intra-X chromosome insertion, and possible position effect in an otherwise normal female.Clin. Genet. 20: 28–35.
Martin, N.J., Cartwright, D.W., and Harvey, P.J. 1985. Duplication 5q(5q22→5q33): From an intrachromosomal insertion.Am. J. Med. Genet. 20: 57–62.
Miller, M., Kaufman, G., Reed, G., Bilenker, R., and Schinzel, A. 1979. Familial, balanced insertional translocation of chromosome 7 leading to offspring with deletion and duplication of the inserted segment, 7q15→7p21.Am. J. Med. Genet. 4: 323–332.
Narahara, K., Takahashi, Y., Kikkawa, K., Wakita, Y., Kimura, S., and Kimoto, H. 1986. Assignment of ABO locus to 9q31.3→qter by study of a family in which an intrachromosomal shift involving chromosome 9 is segregating.Jpn. J. Human Genet. 31: 289–296.
Pai, G.S., Rogers, J.F., and Sommer, A. 1983. Identical multiple congenital anomalies/mental retardation (MCA/MR) syndrome due to del(2) (q32) in two sisters with intrachromosomal insertional translocation in their father.Am. J. Med. Genet. 14: 189–195.
Palmer, C.G., Christian, J.C., and Merritt, A.D. 1977. Partial trisomy 1 due to a “shift” and probable location of the Duffy (Fy) locus.Am. J. Hum. Genet. 29: 371–377.
Pan, S.F., Fatora, S.R., Sorg, R., Garver, K.L., and Steele, M.W. 1977. Meiotic consequences of an intrachromosomal insertion of chromosome No. 1: A family pedigree.Clin. Genet. 12: 303–313.
Strobel, R.J., Riccardi, V.M., Ledbetter, D.H., and Hittner, H.M. 1980. Duplication 11p11.3→14.1 to meiotic crossing-over.Am. J. Med. Genet. 7: 15–20.
Therkelsen, A.J., Hultén, M., Jonasson, J., Lindsten, J., Christensen, N.C., and Iversen, T. 1973. Presumptive direct insertion within chromosome 2 in man.Ann. Hum. Genet. 36: 367–373.
Wyandt, H.E., Kasprzak, R., Ennis, J., Willson, K., Koch, V., Schnatterly, P., Wilson, W., and Kelly, T.E. 1980. Interstitial 3p deletion in a child due to paternal paracentric inserted inversion.Am. J. Hum. Genet. 32: 731–735.
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Narahara, K. Dir ins(9)(q34.3q22.1q31.3) or inv ins(9)(q34.3q22.3q21.2)?. Jap J Human Genet 32, 49–50 (1987). https://doi.org/10.1007/BF01876528
Received:
Published:
Issue date:
DOI: https://doi.org/10.1007/BF01876528
Keywords
This article is cited by
-
Pure partial trisomy of the short arm of chromosome 5
Human Genetics (1989)
