Abstract
A 10 1/2 year old female with skeletal abnormalities was referred for genetic consultation because of learning disabilities and a suggestion of 'Turner-like' stigmata. Cytogenetic analysis revealed a paracentric inversion of an X(q13.1q26.1) chromosome.
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- Ridler M. A., Sutton S. D. A case of a paracentric inversion inv(7)(q11q22). Prenatal detection and counselling. Prenat Diagn. 1981 Jan;1(1):81–84. doi: 10.1002/pd.1970010113. [DOI] [PubMed] [Google Scholar]
- Sarto G. E., Therman E., Patau K. X inactivation in man: a woman with t(Xq--;12q+). Am J Hum Genet. 1973 May;25(3):262–270. [PMC free article] [PubMed] [Google Scholar]
- Summitt R. L., Tipton R. E., Wilroy R. S., Jr, Martens P. R., Phelan J. P. X-autosome translocations: a review. Birth Defects Orig Artic Ser. 1978;14(6C):219–247. [PubMed] [Google Scholar]
- Yunis J. J. High resolution of human chromosomes. Science. 1976 Mar 26;191(4233):1268–1270. doi: 10.1126/science.1257746. [DOI] [PubMed] [Google Scholar]
- del Solar C., Uchida I. A. Identification of chromosomal abnormalities by quinacrine-staining technique in patients with normal karyotypes by conventional analysis. J Pediatr. 1974 Apr;84(4):534–538. doi: 10.1016/s0022-3476(74)80673-6. [DOI] [PubMed] [Google Scholar]


