Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Yurivia Cervantes‐Manzo"'
Autor:
Frank Diaz, Shaweta Khosa, Dmitriy Niyazov, Hane Lee, Richard Person, Michelle M. Morrow, Rebecca Signer, Naghmeh Dorrani, Allison Zheng, Matthew Herzog, Robert Freundlich, Undiagnosed Diseases Network, J. Brandon Birath, Yurivia Cervantes‐Manzo, Julian A. Martinez‐Agosto, Christina Palmer, Stanley F. Nelson, Brent L. Fogel, Shri K. Mishra
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 7, Iss 11, Pp 2320-2325 (2020)
Abstract Exome or genome sequencing was performed to identify the genetic etiology for the clinical presentation of global developmental delay, intellectual disability, and sensorimotor neuropathy with associated distal weakness in two unrelated fami
Externí odkaz:
https://doaj.org/article/a293335fdb084d1fa6a06c767cefacc1
Autor:
Allison Zheng, J Brandon Birath, Frank Diaz, Yurivia Cervantes-Manzo, Richard E. Person, Michelle M. Morrow, Brent L. Fogel, Robert Freundlich, Matthew R. Herzog, Hane Lee, Stanley F. Nelson, Christina G.S. Palmer, Shaweta Khosa, Shri K. Mishra, Dmitriy Niyazov, Rebecca Signer, Naghmeh Dorrani, Julian A. Martinez-Agosto
Publikováno v:
Annals of Clinical and Translational Neurology
Annals of Clinical and Translational Neurology, Vol 7, Iss 11, Pp 2320-2325 (2020)
Annals of Clinical and Translational Neurology, Vol 7, Iss 11, Pp 2320-2325 (2020)
Exome or genome sequencing was performed to identify the genetic etiology for the clinical presentation of global developmental delay, intellectual disability, and sensorimotor neuropathy with associated distal weakness in two unrelated families. A h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::56c67fe24ffbb64f62506c626e83c01a
https://pubmed.ncbi.nlm.nih.gov/33058507
https://pubmed.ncbi.nlm.nih.gov/33058507