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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 

R.V. Lebo

Center for Human Genetics

Department of Pediatrics

Boston University School of Medicine

Boston

USA

[email]@bu.edu

Name/email consistency: high

 
 
 
 
 
 
 

Affiliation

  • Center for Human Genetics, Department of Pediatrics, Boston University School of Medicine, Boston, USA. 2000 - 2001

References

  1. Rett syndrome from quintuple and triple deletions within the MECP2 deletion hotspot region. Lebo, R.V., Ikuta, T., Milunsky, J.M., Milunsky, A. Clin. Genet. (2001) [Pubmed]
  2. Highly polymorphic short tandem repeat analyses clarify complex molecular test results. Lebo, R.V., Maher, T., Farrer, L., Fenerci, E.Y., Milunsky, J.M. Diagn. Mol. Pathol. (2001) [Pubmed]
  3. Rare etiology of autosomal recessive disease in a child with noncarrier parents. Lebo, R.V., Shapiro, L.R., Fenerci, E.Y., Hoover, J.M., Chuang, J.L., Chuang, D.T., Kronn, D.F. Am. J. Hum. Genet. (2000) [Pubmed]
 
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