المؤلفون: Chopra, Sameer S., Leshchiner, Ignaty, Duzkale, Hatice, McLaughlin, Heather, Giovanni, Monica, Zhang, Chengsheng, Stitziel, Nathan, Fingeroth, Joyce D., Joyce, Robin M., Lebo, Matthew, Rehm, Heidi, Vuzman, Dana, Maas, Richard, Sunyaev, Shamil R., Murray, Michael, Cassa, Christopher A.

المساهمون: Department of Medicine, Division of Infectious Diseases and Immunology

المصدر: Molecular genetics and genomic medicine ; 3 ; 5 ; 413-23

مصطلحات موضوعية: CHST11, inherited lymphoproliferative disorder, malignant lymphoproliferative disorder, MIR3922, skeletal malformation, Genomics, Hemic and Lymphatic Diseases, Molecular Genetics, Musculoskeletal Diseases

العلاقة: Link to Article in PubMed; Mol Genet Genomic Med. 2015 Sep;3(5):413-23. doi:10.1002/mgg3.152. Epub 2015 May 10. Link to article on publisher's site; 2324-9269 (Linking); http://hdl.handle.net/20.500.14038/39821Test; https://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=3623&context=oapubs&unstamped=1Test; https://escholarship.umassmed.edu/oapubs/2619Test; 7920037; oapubs/2619

الإتاحة: https://doi.org/10.1002/mgg3.152Test
https://doi.org/20.500.14038/39821Test
https://hdl.handle.net/20.500.14038/39821Test
https://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=3623&context=oapubs&unstamped=1Test
https://escholarship.umassmed.edu/oapubs/2619Test

المؤلفون: Chopra, S.S., Leshchiner, I., Duzkale, H., McLaughlin, H., Giovanni, M., Zhang, C., Cassa, C.A.

المساهمون: Chopra, S.S., Leshchiner, I., Duzkale, H., McLaughlin, H., Giovanni, M., Zhang, C., Cassa, C.A., Yeditepe Üniversitesi

مصطلحات موضوعية: CHST11, Inherited lymphoproliferative disorder, Malignant lymphoproliferative disorder, MIR3922, Skeletal malformation

العلاقة: Molecular Genetics and Genomic Medicine; Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı; 413; 423; https://hdl.handle.net/20.500.11831/1568Test

الإتاحة: https://doi.org/20.500.11831/1568Test
https://hdl.handle.net/20.500.11831/1568Test

المؤلفون: Chopra, SS, Leshchiner, I, Duzkale, H, McLaughlin, H, Giovanni, M, Zhang, CS, Cassa, CA

المساهمون: Chopra, SS, Leshchiner, I, Duzkale, H, McLaughlin, H, Giovanni, M, Zhang, CS, Cassa, CA, Yeditepe Üniversitesi

مصطلحات موضوعية: CHST11, inherited lymphoproliferative disorder, malignant lymphoproliferative disorder, MIR3922, skeletal malformation

العلاقة: MOLECULAR GENETICS & GENOMIC MEDICINE; Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı; WOS: 000214715600006; PubMed ID: 26436107; 413; 423; https://hdl.handle.net/20.500.11831/1571Test

الإتاحة: https://doi.org/20.500.11831/1571Test
https://hdl.handle.net/20.500.11831/1571Test

المؤلفون: Heidi L. Rehm, Dana Vuzman, Sameer S. Chopra, Hatice Duzkale, Matthew S. Lebo, Heather M. McLaughlin, Joyce D. Fingeroth, Chengsheng Zhang, Christopher A. Cassa, Monica A. Giovanni, Richard L. Maas, Ignaty Leshchiner, Michael F. Murray, Nathan O. Stitziel, Shamil R. Sunyaev, Robin Joyce

المصدر: Molecular Genetics & Genomic Medicine

مصطلحات موضوعية: Proband, Genetics, CHST11, Original Articles, Disease, Biology, MIR3922, malignant lymphoproliferative disorder, skeletal malformation, Glycosaminoglycan, Extracellular matrix, chemistry.chemical_compound, inherited lymphoproliferative disorder, chemistry, microRNA, Chondroitin, 1000 Genomes Project, Molecular Biology, Genotyping, Genetics (clinical)

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6aa4cd8adb5c12884db996a515014d0dTest
https://doi.org/10.1002/mgg3.152Test

المؤلفون: Chopra, Sameer S, Leshchiner, Ignaty, Duzkale, Hatice, McLaughlin, Heather, Giovanni, Monica, Zhang, Chengsheng, Stitziel, Nathan, Fingeroth, Joyce, Joyce, Robin M, Lebo, Matthew, Rehm, Heidi, Vuzman, Dana, Maas, Richard, Sunyaev, Shamil R, Murray, Michael, Cassa, Christopher A

مصطلحات موضوعية: inherited lymphoproliferative disorder, malignant lymphoproliferative disorder, skeletal malformation

وصف الملف: application/pdf

العلاقة: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4585449/pdfTest/; Molecular Genetics & Genomic Medicine; Chopra, S. S., I. Leshchiner, H. Duzkale, H. McLaughlin, M. Giovanni, C. Zhang, N. Stitziel, et al. 2015. “Inherited CHST11/MIR3922 deletion is associated with a novel recessive syndrome presenting with skeletal malformation and malignant lymphoproliferative disease.” Molecular Genetics & Genomic Medicine 3 (5): 413-423. doi:10.1002/mgg3.152. http://dx.doi.org/10.1002/mgg3.152Test.; http://nrs.harvard.edu/urn-3:HUL.InstRepos:23473980Test

الإتاحة: https://doi.org/10.1002/mgg3.152Test
http://nrs.harvard.edu/urn-3:HUL.InstRepos:23473980Test

المؤلفون: Chopra, SS, Leshchiner, I, Duzkale, H, McLaughlin, H, Giovanni, M, Zhang, CS, Cassa, CA

المساهمون: Chopra, S.S., Leshchiner, I., Duzkale, H., McLaughlin, H., Giovanni, M., Zhang, C., Cassa, C.A., Yeditepe Üniversitesi, Chopra, SS, Leshchiner, I, Duzkale, H, McLaughlin, H, Giovanni, M, Zhang, CS, Cassa, CA

مصطلحات موضوعية: Malignant lymphoproliferative disorder, CHST11, MIR3922, Skeletal malformation, Inherited lymphoproliferative disorder

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::747f31523dd923944d98cf63678f7456Test
https://hdl.handle.net/20.500.11831/1568Test