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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.
Allderdice, P.W., Kaita, H., Lewis, M., McAlpine, P.J., Wong, P., Anderson, J., and Giblett, E.R. 1986. Segregation of marker loci in families with an inherited paracentric insertion of chromosome 9.Am. J. Hum. Genet. 39: 612–617.
Groupe de Cytogénéticiens Français. 1986. Paracentric inversions in man. A French collaborative study.Ann. Génét. 29: 169–176.
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.
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.
Wyandt, H.E., Kasprzak, R., Ennis, J., Willson, K., Koh, U., Schnatterly, P., Wilson, W., and Kelly, T.E. 1980. Interstitial 3p deletion in a child due to paternal paracentric insertion inversion.Am. J. Hum. Genet. 32: 731–735.
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Kajii, T., Matsuura, S., Murano, I. et al. Inverted insertion (9)(q34.3q22.3q21.2) and its recombination product: Duplication 9q21.2q22.3. Jap J Human Genet 32, 45–48 (1987). https://doi.org/10.1007/BF01876527
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DOI: https://doi.org/10.1007/BF01876527
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