Abstract
A girl with an interstitial deletion of the long arm of chromosome 11 is described. The patient was mildly mentally retarded and showed some facial dysmorphic features, including hypertelorism, ptosis, and cleft palate.
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- Jacobsen P., Hauge M., Henningsen K., Hobolth N., Mikkelsen M., Philip J. An (11;21) translocation in four generations with chromosome 11 abnormalities in the offspring. A clinical, cytogenetical, and gene marker study. Hum Hered. 1973;23(6):568–585. doi: 10.1159/000152624. [DOI] [PubMed] [Google Scholar]
- McPherson E., Meissner L. 11q-syndrome: review and report of two cases. Birth Defects Orig Artic Ser. 1982;18(3B):295–300. [PubMed] [Google Scholar]
- Sørensen K., Nielsen J., Holm V., Haahr J. Fragile site long arm chromosome 16. Hum Genet. 1979 Apr 17;48(1):131–134. doi: 10.1007/BF00273287. [DOI] [PubMed] [Google Scholar]
- van Kessel A. G., Tetteroo P., van Agthoven T., Paulussen R., van Dongen J., Hagemeijer A., von dem Borne A. Localization of human myeloid-associated surface antigen detected by a panel of 20 monoclonal antibodies to the q12-qter region of chromosome 11. J Immunol. 1984 Sep;133(3):1265–1269. [PubMed] [Google Scholar]