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Partial trisomy 16q resulting from maternal translocation

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Summary

A 3 1/2-year-old male with partial trisomy of the long arm of chromosome 16 resulting from a maternal balanced translocation is described. Karyotype: 46,XY,-22,der(22),t(16;22)(q21;p12)mat.

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References

  • Boué, A., Boué, J.: Chromosome abnormalities and abortion. In: Physiology and genetics of reproduction, E. M. Coutinho, F. Fuchs eds., Part B. New York: Plenum 1975

    Google Scholar 

  • Boué, J., Daketse, M. J., Deluchat, C., Yvert, F., Ravisé, N., Boué, A.: Identification par les bandes Q et G des anomalies chromosomiques dans les avortements spontanés. Ann. Genet. (Paris) 19, 233–239 (1976)

    Google Scholar 

  • Eriksson, B., Fraccaro, M., Hulten, H. Lindsten, J., Thoren, C., Tiepolo, L.: Structural abnormalities of chromosome 18. II. Two familial translocations, B/18 and 16/18, ascertained through unbalanced forms. Ann. Genet. (Paris) 14, 281–290 (1971)

    Google Scholar 

  • Fryns, J. P., Melchoir, F., Jaeken, J., van den Berghe, H.: Partial monosomy of the long arm of chromosome 16 in a malformed newborn: Karyotype 46,XX,del(16)(q21). Hum. Genet. 38, 343–346 (1977)

    Google Scholar 

  • Riccardi, V. M., Labhard, M., Marcus, E. S.: Hemihypertrophy with contralateral 16q chromosomal deletion. Am. J. Hum. Genet. 29, 91A (1977)

  • Saadi, A. Al, Yang, S. S., Singla, P.: Partial trisomies of chromosome 22 and 16 in a microphthalmic infant. Am. J. Hum. Genet. 29, 18A (1977)

  • Schmickel, R., Poznanski, A., Himebaugh, J.: 16q trisomy in a family with a balanced 15/16 translocation. Birth Defects XI, No. 5, 229–236 (1975)

    Google Scholar 

  • Stern, L. M., Murch, A. R.: Pseudohermaphroditism with clinical features of trisomy 18 in an infant trisomic for parts of chromosome 16 and 18: 47,XY,der(18)t(16;18)(p12;q11)mat. J. Med. Genet. 12, 305–307 (1975)

    Google Scholar 

  • Yunis, E., Gonzales, J. T., Torres de Caballero, O. M.: Partial trisomy 16q. Hum. Genet. 38, 347–350 (1977)

    Google Scholar 

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Balestrazzi, P., Giovannelli, G., Rubini, L.L. et al. Partial trisomy 16q resulting from maternal translocation. Hum Genet 49, 229–235 (1979). https://doi.org/10.1007/BF00277648

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  • DOI: https://doi.org/10.1007/BF00277648

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