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

Cheryl L. Maslen

Department of Medicine

Oregon Health and Science University

Portland Oregon 97239

USA

[email]@ohsu.edu

Name/email consistency: high

 
 
 
 
 
 
 

Affiliation

  • Department of Medicine, Oregon Health and Science University, Portland Oregon 97239, USA. 1997 - 2006

References

  1. CRELD2: gene mapping, alternate splicing, and comparative genomic identification of the promoter region. Maslen, C.L., Babcock, D., Redig, J.K., Kapeli, K., Akkari, Y.M., Olson, S.B. Gene (2006) [Pubmed]
  2. CRELD1 mutations contribute to the occurrence of cardiac atrioventricular septal defects in Down syndrome. Maslen, C.L., Babcock, D., Robinson, S.W., Bean, L.J., Dooley, K.J., Willour, V.L., Sherman, S.L. Am. J. Med. Genet. A (2006) [Pubmed]
  3. Molecular genetics of atrioventricular septal defects. Maslen, C.L. Curr. Opin. Cardiol. (2004) [Pubmed]
  4. A rare branch-point mutation is associated with missplicing of fibrillin-2 in a large family with congenital contractural arachnodactyly. Maslen, C., Babcock, D., Raghunath, M., Steinmann, B. Am. J. Hum. Genet. (1997) [Pubmed]
 
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