Inherited CHST11/MIR3922 deletion is associated with a novel recessive syndrome presenting with skeletal malformation and malignant lymphoproliferative disease. Chopra, S. S, Leshchiner, I., Duzkale, H., McLaughlin, H., Giovanni, M., Zhang, C., Stitziel, N., Fingeroth, J., Joyce, R. M, Lebo, M., & others Molecular Genetics & Genomic Medicine, 3(5):413–423, 2015.
bibtex   
@article{chopra2015inherited,
  title={Inherited CHST11/MIR3922 deletion is associated with a novel recessive syndrome presenting with skeletal malformation and malignant lymphoproliferative disease},
  author={Chopra, Sameer S and Leshchiner, Ignaty and Duzkale, Hatice and McLaughlin, Heather and Giovanni, Monica and Zhang, Chengsheng and Stitziel, Nathan and Fingeroth, Joyce and Joyce, Robin M and Lebo, Matthew and others},
  journal={Molecular Genetics \& Genomic Medicine},
  volume={3},
  number={5},
  pages={413--423},
  year={2015}
}

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