Literature DB >> 2881272

A highly polymorphic locus in 5p15.2-5p15.3 (213-274EC) revealed by an anonymous single copy DNA fragment.

J Overhauser, A L Beaudet, J J Wasmuth.   

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Year:  1987        PMID： 2881272      PMCID： PMC340543          DOI： 10.1093/nar/15.3.1345

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN： 0305-1048            Impact factor:   16.971


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  1 in total

1.  Molecular approach to analyzing the human 5p deletion syndrome, cri du chat.

Authors:  L R Carlock; J J Wasmuth
Journal:  Somat Cell Mol Genet       Date:  1985-05
  1 in total
  1 in total

1.  Uniparental disomy as a mechanism for human genetic disease.

Authors:  J E Spence; R G Perciaccante; G M Greig; H F Willard; D H Ledbetter; J F Hejtmancik; M S Pollack; W E O'Brien; A L Beaudet
Journal:  Am J Hum Genet       Date:  1988-02       Impact factor: 11.025
  1 in total

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