Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Troy, Jenkins"'
Autor:
Conner Jenkins, Troy Jenkins, Thomas N Person, Peter N Robinson, Alanna Kulchak Rahm, Nephi A Walton, Lynn K Feldman, Joeseph Peterson, Jonathon C Reynolds, Makenzie A Woltz, Marc S Williams, Michael M Segal
Publikováno v:
BMJ Health & Care Informatics, Vol 28, Iss 1 (2021)
Objectives There is a need in clinical genomics for systems that assist in clinical diagnosis, analysis of genomic information and periodic reanalysis of results, and can use information from the electronic health record to do so. Such systems should
Externí odkaz:
https://doaj.org/article/6f81dbb812864747af76481cc3b38917
Autor:
Carol Wise, Darren K. Johnson, Lilian Antunes, Cathleen L. Raggio, Todd E. Druley, Conner Jenkins, Mark A. Seeley, R. Spencer Tong, Nephi A. Walton, Nancy H. Miller, Matthew T. Oetjens, Jose A. Morcuende, Xavier Bledsoe, Christina A. Gurnett, Gabe Haller, Brooke Sadler, Ina E Amarillo, Matthew B. Dobbs, Yared H. Kidane, Philip F. Giampietro, Troy Jenkins
Publikováno v:
Journal of Medical Genetics. 56:427-433
IntroductionAdolescent idiopathic scoliosis (AIS) is a common musculoskeletal disorder with strong evidence for a genetic contribution. CNVs play an important role in congenital scoliosis, but their role in idiopathic scoliosis has been largely unexp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::30fadeac2be52dbf977b9c38bae98fc8
https://doi.org/10.1136/jmedgenet-2018-105877
https://doi.org/10.1136/jmedgenet-2018-105877
Autor:
Brooke, Sadler, Gabe, Haller, Lilian, Antunes, Xavier, Bledsoe, Jose, Morcuende, Philip, Giampietro, Cathleen, Raggio, Nancy, Miller, Yared, Kidane, Carol A, Wise, Ina, Amarillo, Nephi, Walton, Mark, Seeley, Darren, Johnson, Conner, Jenkins, Troy, Jenkins, Matthew, Oetjens, R Spencer, Tong, Todd E, Druley, Matthew B, Dobbs, Christina A, Gurnett
Publikováno v:
Journal of medical genetics. 56(7)
INTRODUCTION: Adolescent idiopathic scoliosis (AIS) is a common musculoskeletal disorder with strong evidence for a genetic contribution. Copy number variants (CNVs) play an important role in congenital scoliosis, but their role in idiopathic scolios
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6bce11cce7d3c512d5a9fdbd29a52422
https://pubmed.ncbi.nlm.nih.gov/30803986
https://pubmed.ncbi.nlm.nih.gov/30803986