Summary
Clinical findings of partial trisomy 11p are described in a patient bearing t(3;11;20) (p13;p11;q13). The translocation was present in balanced form in her mother (46,XX)t(3;11;20)(p13;p11;q13).
References
Allerdice, P. W., Miller, O. J., Miller, D. A., Breg, W. R., Gendel, E., Zelson, C.: Familial tramslocation involving chromosomes 6, 14 and 20, identified by quinacrine fluorescence. Humangenetik 13, 205–209 (1971)
Bobrow, M., Jones, J. F., Clarke, G.: A complex chromosomal rearrangement with formation of a ring 4. J. med. Genet. 8, 235–239 (1971)
Catti, A., Schmid, W.: A pericentric inversion, 5p-q+, and additional complex rearrangements in a case of Cri-du-Chat syndrome. Cytogenetics 10, 50–60 (1971)
Creasy, M. R., Crolla, J. A., Daker, M. G.: A familial reciprocal translocation between three chromosomes. Humangenetik 24, 303–308 (1974)
de Grouchy, J., Lautmann, F.: Caryotype 46,XX,1q-,2q-,Dq+,16q+ chez une infant polymalformee. Ann. Génét. 11, 129–131 (1968)
Falk, R. E., Carel, R. E., Valente, M., Crandall, B. F., Sparkes, R. S.: Partial trisomy of chromosome 11: A case report. Amer. J. ment. Defic. 77, 383–388 (1973)
Fitzgerald, M. G.: Complex five break rearrangement. Clin. Genet. 5, 62–67 (1974)
Fredga, K., Hall, B.: A complex familial translocation involving chromosomes 5, 19, 13. Cytogenetics 9, 294–306 (1970)
Fujita, H., Abe, T., Yamamoto, K., Furuyama, J.: Possible complex translocation t(9;14;13) (q12;pl?;q31) in mother of a child with 9p- trisomy syndrome. Humangenetik 25, 83–92 (1974)
Martinetti, J., Noel, B.: Complex de-novo rearrangement involving 4 chromosomes in a newborn. Ann. Génét. 16, 285–288 (1973)
Nuzzo, F., Marini, A., Baglioni, C., Ford, C. E., deCarli, L., Sereni, L. P.: A case of multiple chromosomal rearrangements with persistence of foetal hemoglobin. Cytogenetics 7, 169–182 (1968)
Sanchez, O., Yunis, J. J., Escobar, J. I.: Partial trisomy 11 in a child resulting from a complex maternal rearrangement of chromosomes 11, 12 and 13. Humangenetik 22, 59–65 (1974)
Schwinger, E., Mikkelsen, M., Niesen, M.: Familial balanced (7;11;21) translocation and Down's syndrome in two siblings. Clin. Genet. 7, 304 (1975)
Taillemete, J. L., Baheux-Morlier, G., Cathelineau, L., Roux, C.: Cri-du-Chat syndrome and complex chromosome rearrangement in a dizygotic twin. Ann. Génét. 16, 127–130 (1973)
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Palmer, C.G., Poland, C., Reed, T. et al. Partial trisomy 11,46,XX,-3,-20,+der3,+der20,t(3:11:20), resulting from a complex maternal rearrangement of chromosomes 3, 11, 20. Hum Genet 31, 219–225 (1976). https://doi.org/10.1007/BF00296149
Received:
Issue Date:
DOI: https://doi.org/10.1007/BF00296149