Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Stephanie Hallam"'
Autor:
Stephanie Hallam, Pat Willingham
Publikováno v:
MethodsX, Vol 9, Iss , Pp 101612- (2022)
This method utilizes a template for an open pedagogy lesson plan using US government documents that can be applied to academic levels ranging from elementary to post-secondary. This method addresses concerns about OER quality, exposes students to the
Externí odkaz:
https://doaj.org/article/a7c16799312545038e56a46a1329e131
Publikováno v:
College & Undergraduate Libraries. 28:51-66
Kent Library at Southeast Missouri State University is one of the only academic libraries in the United States to have a faculty-selected main collection. Three newly hired employees to the library...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c005768ab5747fffedc17e2ff90937a2
https://doi.org/10.1080/10691316.2021.1885548
https://doi.org/10.1080/10691316.2021.1885548
Autor:
Stephanie Hallam, Pat Willingham
Publikováno v:
MethodsX
MethodsX, Vol 9, Iss, Pp 101612-(2022)
MethodsX, Vol 9, Iss, Pp 101612-(2022)
This method utilizes a template for an open pedagogy lesson plan using US government documents that can be applied to academic levels ranging from elementary to post-secondary. This method addresses concerns about OER quality, exposes students to the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::90d643865e8ff1af8dcb5e8d7baeef75
https://pubmed.ncbi.nlm.nih.gov/35004233
https://pubmed.ncbi.nlm.nih.gov/35004233
Publikováno v:
The Journal of Academic Librarianship. 47:102358
An education information librarian, a government documents librarian, and an instructional designer collaboratively developed a lesson plan to engage researchers with open educational resources (OER). They selected and curated freely available, onlin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5d2240c61d3d85589e933c96c0d7c0c1
https://doi.org/10.1016/j.acalib.2021.102358
https://doi.org/10.1016/j.acalib.2021.102358
Autor:
Pranil Chandra, Elaine Lyon, Roger D. Klein, Jill M. Hagenkord, Milena Cankovic, Rajyasree Emmadi, Paul G. Rothberg, Kay E. Jewell, Robyn L. Temple-Smolkin, Samuel Caughron, Victoria M. Pratt, Stephanie Hallam, Loren Joseph
Publikováno v:
The Journal of Molecular Diagnostics. 18:605-619
Clinical utility describes the benefits of each laboratory test for that patient. Many stakeholders have adopted narrow definitions for the clinical utility of molecular testing as applied to targeted pharmacotherapy in oncology, regardless of the po
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::042d6d6ba37484be7dcedbb97ac0998a
https://doi.org/10.1016/j.jmoldx.2016.05.007
https://doi.org/10.1016/j.jmoldx.2016.05.007
Autor:
Valerie Greger, Dana Neitzel, Cynthia Perreault-Micale, Jessica Sullivan, Nicole Faulkner, Stephanie Hallam, Alexander Frieden, Caleb J. Kennedy
Publikováno v:
The Journal of Molecular Diagnostics. 16(6):673-678
Loss of function variants in the PCDH15 gene can cause Usher syndrome type 1F, an autosomal recessive disease associated with profound congenital hearing loss, vestibular dysfunction, and retinitis pigmentosa. The Ashkenazi Jewish population has an i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::51dca9d2b8828c32f40418a9ad59ecf4
Autor:
Loren, Joseph, Milena, Cankovic, Samuel, Caughron, Pranil, Chandra, Rajyasree, Emmadi, Jill, Hagenkord, Stephanie, Hallam, Kay E, Jewell, Roger D, Klein, Victoria M, Pratt, Paul G, Rothberg, Robyn L, Temple-Smolkin, Elaine, Lyon
Publikováno v:
The Journal of molecular diagnostics : JMD. 18(5)
Clinical utility describes the benefits of each laboratory test for that patient. Many stakeholders have adopted narrow definitions for the clinical utility of molecular testing as applied to targeted pharmacotherapy in oncology, regardless of the po
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::142e91789e465284c9fa33f0d3f76614
https://pubmed.ncbi.nlm.nih.gov/27542512
https://pubmed.ncbi.nlm.nih.gov/27542512
Publikováno v:
Molecular Genetics & Genomic Medicine
Carrier screening for certain diseases is recommended by major medical and Ashkenazi Jewish (AJ) societies. Most carrier screening panels test only for common, ethnic-specific variants. However, with formerly isolated ethnic groups becoming increasin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::016bd10f18a3905bcc8a19821941241c
https://pubmed.ncbi.nlm.nih.gov/26247052
https://pubmed.ncbi.nlm.nih.gov/26247052
Publikováno v:
Genetics in Medicine. 7:246-250
Purpose: To document our experience with fragile X carrier screening. Methods: In this study, 29,103 women with no known or suspected family history of fragile X syndrome were offered fragile X carrier screening during their prenatal genetic counseli
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d8603e5c71b187679f798606bbadc4a1
https://doi.org/10.1097/01.gim.0000159898.90221.d3
https://doi.org/10.1097/01.gim.0000159898.90221.d3