Interstitial deletion of chromosome 13 and associated congenital anomalies

Allderdice, P. W., Davis, J. G., Miller, O. J., Klinger, H. P., Warburton, D., Miller, D. A., Allen, F. H., Abrams, A. L., McGilray, E.: The 13q- deletion syndrome. Am. J. Hum. Genet. 21, 499–512 (1969)

Cross, H. E., Hansen, R. C., Morrow, G., Davis, J. R.: Retinoblastoma in a patient with a 13qXp translocation. Am. J. Ophthalmol. 84, 548–554 (1977)

Cuschieri, A., Agius, P. V., Scheres, J. M. J. C.: Partial deletion of the long arm of chromosome No. 13. Hum. Genet. 36, 341–344 (1977)

Francke, U.: Retinoblastoma and chromosome 13. Cytogenet. Cell Genet. 16 (1–5), 131–134 (1976)

Francke, U., Kung, F.: Sporadic bilateral retinoblastoma and 13q- chromosomal deletion. Med. Ped. Oncol. 2, 379–385 (1976)

Fryns, J. P., Deroover, J., Van den Berghe, H.: Malformative syndrome with ring chromosome 13. Humangenetik 24, 235–240 (1974)

Grosse, K. P., Schwanitz, G.: Ein neues Syndrom durch Chromosomenstrukturverlust (13q). Kasuistik und Zusammenstellung der Symptomatik. Klin. Pediat. 185, 468–473 (1973)

Howard, R. O., Breg, W. R., Albert, D. M., Lesser, R. L.: Retinoblastoma and chromosome abnormality. Arch. Ophthalmol. 92, 490–493 (1974)

Ikeuchi, T., Sonta, S., Sasaki, M., Hujita, M., Tsunematsu, K.: Chromosome banding patterns in an infant with 13q- syndrome. Humangenetik 21, 309–313 (1974)

Knudson, A. G., Meadows, A. T., Nichols, W. W., Hill, R. B.: Chromosomal deletion and retinoblastoma. N. Engl. J. Med. 295, 1120–1123 (1976)

Kucerova, M., Polivkova, A., Pokorna, M.: Deletion of long arms of chromosome 13. Human-genetik 27, 255–275 (1975)

Lejeune, J., Lafourcade, J., Berger, R., Cruveiller, J., Rethoré, M. O., Dutrillaux, B., Abonyi, D., Jerôme, J.: I. e phenotype (Dr.) etude de trois case de chromosome D en anneau. Ann. Génét. 11, 79 (1968)

Lewandowski, R. C., Yunis, J. J.: New chromosomal syndromes. Am. J. Dis. Child. 129, 515–529 (1975)

Niebuhr, E.: Partial trisomies and deletions of chromosome 13. In: New chromosomal syndromes, J. J. Yunis, ed., pp. 273–279. New York: Academic Press 1977

Niebuhr, E., Ottosen, J.: Ring chromosome D (13) associated with multiple congenital malformations. Ann. Génét. 16, 157–166 (1973)

Noel, B., Quack, B., Rethoré, M. O.: Partial deletions and trisomies of chromosome 13; mapping of bands associated with particular malformations. Clin. Genet. 9, 593–602 (1976)

Nomoto, Y., Miyaji, F., Maeda, K., Nakayama, Y., Shike, S., Shinohara, T., Miyata, H.: A case of chromosome abnormality with 13q-. Jpn. J. Hum. Genet. 19, 78–79 (1974)

Orbeli, D. J., Lurie, I. W., Goroshenko, J. L.: The syndrome associated with the partial D-monosomy. Humangenetik 13, 296–308 (1971)

Orye, E., Delbeke, M. J., Vandenabeele, B.: Retinoblastoma and long arm deletion of chromosome 13. Attempts to define the deleted segment. Clin. Genet. 5, 458–465 (1974)

Riccardi, V. M., Hittner, H. M., Francke, U., Pippin, S., Holmquist, G. P., Kretzer, F. L., Ferrell, R.: Partial triplication and deletion of 13q: study of a family presenting with bilateral retinoblastoma. Clin. Genet. 15, 332–345 (1979)

Seabright, M. A.: A rapid banding technique for human chromosomes. Lancet II, 971–972 (1971)

Sparkes, R. S., Muller, H., Klisak, I., Abram, J. A.: Retinoblastoma with 13q- chromosomal deletion associated with maternal paracentric inversion of 13q. Science 203, 1027–1029 (1979)

Wilson, M. G., Ebbin, A. J., Towner, J. W., Spencer, W. H.: Chromosomal anomalies in patients with retinoblastoma. Clin. Genet. 12, 1–8 (1977)

Wilson, M. G., Ebbin, J. W., Spencer, W. H.: Chromosome abnormalities in patients with retinoblastoma. Am. J. Hum. Genet. 27, 95A 91975

Wilson, M. G., Towner, J. W., Fujimoto, A.: Retinoblastoma and D-chromosome deletion. Am. J. Hum. Genet. 25, 57–61 (1973)

Yunis, J. J., Ramsay, N.: Retinoblastoma and subband deletion of chromosome 13. Am. J. Dis. Child. 132, 161–163 (1978)