Abstract
A terminal deletion of chromosome 3 at p25.3 was observed during prenatal diagnosis. A similar deletion is also present in the phenotypically normal mother. The deletion was confirmed by FISH. The breakpoint is distal to the region responsible for the 3p- syndrome. A normal baby girl was born with no apparent phenotypic abnormalities.
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- Asai M., Ito Y., Iguchi T., Ito J., Okada N., Oishi H. Terminal deletion of the short arm of chromosome 3. Jpn J Hum Genet. 1992 Jun;37(2):163–168. doi: 10.1007/BF01899740. [DOI] [PubMed] [Google Scholar]
- Nienhaus H., Mau U., Zang K. D. Infant with del(3) (p25-pter): karyotype-phenotype correlation and review of previously reported cases. Am J Med Genet. 1992 Nov 15;44(5):573–575. doi: 10.1002/ajmg.1320440508. [DOI] [PubMed] [Google Scholar]
- Phipps M. E., Latif F., Prowse A., Payne S. J., Dietz-Band J., Leversha M., Affara N. A., Moore A. T., Tolmie J., Schinzel A. Molecular genetic analysis of the 3p- syndrome. Hum Mol Genet. 1994 Jun;3(6):903–908. doi: 10.1093/hmg/3.6.903. [DOI] [PubMed] [Google Scholar]