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Diagnostic utility of transcriptome sequencing for rare Mendelian diseases

Diagnostic utility of transcriptome sequencing for rare Mendelian diseases

Lee, Hane; Huang, Alden Y.; Wang, Lee-kai; Yoon, Amanda J.; Renteria, Genecee; Eskin, Ascia; Signer, Rebecca H.; Dorrani, Naghmeh; Nieves-Rodriguez, Shirley; Wan, Jijun; Douine, Emilie D.; Woods, Jeremy D.; Dell’Angelica, Esteban C.; Fogel, Brent L.; Martin, Martin G.; Butte, Manish J.; Parker, Neil H.; Wang, Richard T.; Shieh, Perry B.; Wong, Derek A.; Gallant, Natalie; Singh, Kathryn E.; Tavyev Asher, Y. Jane; Sinsheimer, Janet S.; Krakow, Deborah; Loo, Sandra K.; Allard, Patrick; Papp, Jeanette C.; Palmer, Christina G. S.; Martinez-Agosto, Julian A.; Nelson, Stanley F.
  • 期刊名称Genetics in Medicine
  • 作者Lee, Hane; Huang, Alden Y.; Wang, Lee-kai; Yoon, Amanda J.; Renteria, Genecee; Eskin, Ascia; Signer, Rebecca H.; Dorrani, Naghmeh; Nieves-Rodriguez, Shirley; Wan, Jijun; Douine, Emilie D.; Woods, Jeremy D.; Dell’Angelica, Esteban C.; Fogel, Brent L.; Martin, Martin G.; Butte, Manish J.; Parker, Neil H.; Wang, Richard T.; Shieh, Perry B.; Wong, Derek A.; Gallant, Natalie; Singh, Kathryn E.; Tavyev Asher, Y. Jane; Sinsheimer, Janet S.; Krakow, Deborah; Loo, Sandra K.; Allard, Patrick; Papp, Jeanette C.; Palmer, Christina G. S.; Martinez-Agosto, Julian A.; Nelson, Stanley F.
  • 印刷ISSN1098-3600
  • 电子ISSN1530-0366
  • 文件大小648.69KB
  • 发表时间2019-10-14
  • DOI10.1038/s41436-019-0672-1
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