{"_id":"Gko4HS5fy789ZLnwu","bibbaseid":"chopra-leshchiner-duzkale-mclaughlin-giovanni-zhang-stitziel-fingeroth-etal-inheritedchst11mir3922deletionisassociatedwithanovelrecessivesyndromepresentingwithskeletalmalformationandmalignantlymphoproliferativedisease-2015","author_short":["Chopra, S. S","Leshchiner, I.","Duzkale, H.","McLaughlin, H.","Giovanni, M.","Zhang, C.","Stitziel, N.","Fingeroth, J.","Joyce, R. M","Lebo, M.","others"],"bibdata":{"bibtype":"article","type":"article","title":"Inherited CHST11/MIR3922 deletion is associated with a novel recessive syndrome presenting with skeletal malformation and malignant lymphoproliferative disease","author":[{"propositions":[],"lastnames":["Chopra"],"firstnames":["Sameer","S"],"suffixes":[]},{"propositions":[],"lastnames":["Leshchiner"],"firstnames":["Ignaty"],"suffixes":[]},{"propositions":[],"lastnames":["Duzkale"],"firstnames":["Hatice"],"suffixes":[]},{"propositions":[],"lastnames":["McLaughlin"],"firstnames":["Heather"],"suffixes":[]},{"propositions":[],"lastnames":["Giovanni"],"firstnames":["Monica"],"suffixes":[]},{"propositions":[],"lastnames":["Zhang"],"firstnames":["Chengsheng"],"suffixes":[]},{"propositions":[],"lastnames":["Stitziel"],"firstnames":["Nathan"],"suffixes":[]},{"propositions":[],"lastnames":["Fingeroth"],"firstnames":["Joyce"],"suffixes":[]},{"propositions":[],"lastnames":["Joyce"],"firstnames":["Robin","M"],"suffixes":[]},{"propositions":[],"lastnames":["Lebo"],"firstnames":["Matthew"],"suffixes":[]},{"firstnames":[],"propositions":[],"lastnames":["others"],"suffixes":[]}],"journal":"Molecular Genetics & Genomic Medicine","volume":"3","number":"5","pages":"413–423","year":"2015","bibtex":"@article{chopra2015inherited,\n title={Inherited CHST11/MIR3922 deletion is associated with a novel recessive syndrome presenting with skeletal malformation and malignant lymphoproliferative disease},\n 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},\n journal={Molecular Genetics \\& Genomic Medicine},\n volume={3},\n number={5},\n pages={413--423},\n year={2015}\n}\n\n","author_short":["Chopra, S. S","Leshchiner, I.","Duzkale, H.","McLaughlin, H.","Giovanni, M.","Zhang, C.","Stitziel, N.","Fingeroth, J.","Joyce, R. M","Lebo, M.","others"],"key":"chopra2015inherited","id":"chopra2015inherited","bibbaseid":"chopra-leshchiner-duzkale-mclaughlin-giovanni-zhang-stitziel-fingeroth-etal-inheritedchst11mir3922deletionisassociatedwithanovelrecessivesyndromepresentingwithskeletalmalformationandmalignantlymphoproliferativedisease-2015","role":"author","urls":{},"metadata":{"authorlinks":{}}},"bibtype":"article","biburl":"https://bibbase.org/network/files/aX4e85mNvLnP28bmF","dataSources":["9CnzWbeQFsvTLJme6","N3rXpkDkdbEvNCA76","hky9vNrwc9uGBMQ9h"],"keywords":[],"search_terms":["inherited","chst11","mir3922","deletion","associated","novel","recessive","syndrome","presenting","skeletal","malformation","malignant","lymphoproliferative","disease","chopra","leshchiner","duzkale","mclaughlin","giovanni","zhang","stitziel","fingeroth","joyce","lebo","others"],"title":"Inherited CHST11/MIR3922 deletion is associated with a novel recessive syndrome presenting with skeletal malformation and malignant lymphoproliferative disease","year":2015}