18p- Syndrome resulting from 14q/18q ?dicentric? fusion translocation

Author:

Funderburk Steve J.,Sparkes Robert S.,Klisak Ivana

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Reference16 articles.

1. Arrighi, F. E., Hsu, T. C.: Localization of heterochromatin in human chromosomes. Cytogenetics 10, 81?86 (1971)

2. Cohen, M. M., Putnam, T. I.: An 18q21q translocation in a patient with presumptive ?monosomy G?. Am. J. Dis. Child. 124, 908?910 (1972)

3. Daniel, A., Lam-Po-Tang, P. R. L. C.: Structure and inheritance of some heterozygous Robertsonian translocations in man. J. Med. Genet. 13, 381?388 (1976)

4. Faust, J., Habedank, M., Nieuwenhuijsen, C.: The 18p- syndrome; Report of four cases. Eur. J. Pediatr. 123, 59?66 (1976)

5. Fraccaro, M., Herin, P., Hultén, M., Ivemark, B. I., Jonasson, J., Lindsten, J., Tiepolo, L., Zetterqvist, P.: Structural abnormalities of chromosome 18. III. Two G/18 translocations, one identified as 22/18. Ann. Génét. 15 93?98 (1972)

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