Tamim Shaikh

Summary

Affiliation: University of Colorado Denver
Country: USA

Publications

  1. pmc Genes and biological processes commonly disrupted in rare and heterogeneous developmental delay syndromes
    Tamim H Shaikh
    Division of Human Genetics, The Children s Hospital of Philadelphia, Philadelphia, PA, USA
    Hum Mol Genet 20:880-93. 2011

Research Grants

  1. Evolution of Chromosome-specific Low Copy Repeats
    Tamim Shaikh; Fiscal Year: 2005
  2. Copy Number Alterations in Genomic Disorders
    Tamim H Shaikh; Fiscal Year: 2010
  3. Copy Number Alterations in Genomic Disorders
    Tamim H Shaikh; Fiscal Year: 2009
  4. Copy Number Alterations in Genomic Disorders
    Tamim H Shaikh; Fiscal Year: 2009

Detail Information

Publications1

  1. pmc Genes and biological processes commonly disrupted in rare and heterogeneous developmental delay syndromes
    Tamim H Shaikh
    Division of Human Genetics, The Children s Hospital of Philadelphia, Philadelphia, PA, USA
    Hum Mol Genet 20:880-93. 2011
    ..These results demonstrate the high predictive potential of model organism phenotypes when implicating candidate genes for rare genomic disorders...

Research Grants9

  1. Evolution of Chromosome-specific Low Copy Repeats
    Tamim Shaikh; Fiscal Year: 2005
    ..Thus, the 22q11 LCRs provide a model system with which to gain a better understanding of the evolution of the human genome. ..
  2. Copy Number Alterations in Genomic Disorders
    Tamim H Shaikh; Fiscal Year: 2010
    ..The identification of genomic regions that are deleted or duplicated in patients with birth defects will allow the identification of genes that are important in normal development. ..
  3. Copy Number Alterations in Genomic Disorders
    Tamim H Shaikh; Fiscal Year: 2009
    ..The identification of genomic regions that are deleted or duplicated in patients with birth defects will allow the identification of genes that are important in normal development. ..
  4. Copy Number Alterations in Genomic Disorders
    Tamim H Shaikh; Fiscal Year: 2009
    ..The identification of genomic regions that are deleted or duplicated in patients with birth defects will allow the identification of genes that are important in normal development. ..