Abstract
A case of partial trisomy 17 with partial monosomy X resulting from a maternal X-autosomal translocation t(X;17)(q13;q21) is presented. Three previously reported cases are reviewed and the phenotypic features of trisomy 17 are discussed.
Full text
PDF




Images in this article
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Dutrillaux B., Fosse A. M. Sur le mécanisme de la segmentation chromosomique induite par le BUDR (5-bromodéoxyuridine) Ann Genet. 1974 Sep;17(3):207–211. [PubMed] [Google Scholar]
- Latta E., Hoo J. J. Trisomy of the short arm of chromosome 17. Humangenetik. 1974;23(3):213–217. doi: 10.1007/BF00285107. [DOI] [PubMed] [Google Scholar]
- Ohama K., Kusumi I., Ihara T. Trisomy 17 in two abortuses. Jinrui Idengaku Zasshi. 1977 Mar;21(4):257–260. [PubMed] [Google Scholar]
- Palutke W., Chen H., Woolley P., Jr, Espiritu C., Vogel H. L., Gohle N., Tyrkus M. An extra small metacentric chromosome identified as a deleted chromosome no. 17. Clin Genet. 1976 May;9(5):454–458. doi: 10.1111/j.1399-0004.1976.tb01596.x. [DOI] [PubMed] [Google Scholar]
- Salamanca-Gómez F., Armendares S. Identification of isochromosome 17 in a girl with mental retardation and congenital malformations. Ann Genet. 1975 Dec;18(4):235–238. [PubMed] [Google Scholar]



