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Alison M. Elliott

Department of Biochemistry and Medical Genetics

University of Manitoba

770 Bannatyne Avenue

Winnipeg

Canada

[email]@mts.net

Name/email consistency: high

 
 
 
 
 
 
 

Affiliation

  • Department of Biochemistry and Medical Genetics, University of Manitoba, 770 Bannatyne Avenue, Winnipeg, Canada. 2004 - 2007

References

  1. Triphalangeal thumb in association with split hand/foot: a phenotypic marker for SHFM3?. Elliott, A.M., Reed, M.H., Evans, J.A. Birth Defects Res. Part A Clin. Mol. Teratol. (2007) [Pubmed]
  2. Clinical and epidemiological findings in patients with central ray deficiency: split hand foot malformation (SHFM) in Manitoba, Canada. Elliott, A.M., Reed, M.H., Chudley, A.E., Chodirker, B.N., Evans, J.A. Am. J. Med. Genet. A (2006) [Pubmed]
  3. Genotype-phenotype correlations in mapped split hand foot malformation (SHFM) patients. Elliott, A.M., Evans, J.A. Am. J. Med. Genet. A (2006) [Pubmed]
  4. Osteocraniostenosis-hypomineralized skull with gracile long bones and splenic hypoplasia. Four new cases with distinctive chondro-osseous morphology. Elliott, A.M., Wilcox, W.R., Spear, G.S., Field, F.M., Steffensen, T.S., Friedman, B.D., Rimoin, D.L., Lachman, R.S. Am. J. Med. Genet. A (2006) [Pubmed]
  5. Discrepancies in upper and lower limb patterning in split hand foot malformation. Elliott, A.M., Reed, M.H., Roscioli, T., Evans, J.A. Clin. Genet. (2005) [Pubmed]
  6. The duplicated longitudinal epiphysis or "kissing delta phalanx": evolution and variation in three different disorders. Elliott, A.M., Evans, J.A., Chudley, A.E., Reed, M.H. Skeletal Radiol. (2004) [Pubmed]
 
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