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. 1987 Jul;24(7):410–412. doi: 10.1136/jmg.24.7.410

Wolf-Hirschhorn locus is distal to D4S10 on short arm of chromosome 4.

C McKeown, A P Read, A Dodge, O Stecko, A Mercer, R Harris
PMCID: PMC1050148  PMID: 3612716

Abstract

We report a family in which Wolf-Hirschhorn syndrome in two children with partial monosomy of the short arm of chromosome 4 is the result of unbalanced segregation of a reciprocal 4;12 translocation in the mother. Studies with the DNA probe G8 show that the translocation breakpoint in this family is distal to the D4S10 locus. Previously reported cases of Wolf-Hirschhorn syndrome have involved the deletion of D4S10. These observations may prove helpful in the search for better genetic markers for Huntington's chorea, which maps close to D4S10.

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Selected References

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  1. Gusella J. F., Tanzi R. E., Bader P. I., Phelan M. C., Stevenson R., Hayden M. R., Hofman K. J., Faryniarz A. G., Gibbons K. Deletion of Huntington's disease-linked G8 (D4S10) locus in Wolf-Hirschhorn syndrome. Nature. 1985 Nov 7;318(6041):75–78. doi: 10.1038/318075a0. [DOI] [PubMed] [Google Scholar]
  2. Gusella J. F., Wexler N. S., Conneally P. M., Naylor S. L., Anderson M. A., Tanzi R. E., Watkins P. C., Ottina K., Wallace M. R., Sakaguchi A. Y. A polymorphic DNA marker genetically linked to Huntington's disease. Nature. 1983 Nov 17;306(5940):234–238. doi: 10.1038/306234a0. [DOI] [PubMed] [Google Scholar]
  3. Kunkel L. M., Monaco A. P., Middlesworth W., Ochs H. D., Latt S. A. Specific cloning of DNA fragments absent from the DNA of a male patient with an X chromosome deletion. Proc Natl Acad Sci U S A. 1985 Jul;82(14):4778–4782. doi: 10.1073/pnas.82.14.4778. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Stengel-Rutkowski S., Warkotsch A., Schimanek P., Stene J. Familial Wolf's syndrome with a hidden 4p deletion by translocation of an 8p segment. Unbalanced inheritance from a maternal translocation (4;8)(p15.3;p22). Case report, review and risk estimates. Clin Genet. 1984 Jun;25(6):500–521. doi: 10.1111/j.1399-0004.1984.tb00494.x. [DOI] [PubMed] [Google Scholar]
  5. Wilson M. G., Towner J. W., Coffin G. S., Ebbin A. J., Siris E., Brager P. Genetic and clinical studies in 13 patients with the Wolf-Hirschhorn syndrome [del(4p)]. Hum Genet. 1981;59(4):297–307. doi: 10.1007/BF00295461. [DOI] [PubMed] [Google Scholar]

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