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BMC Health Services Research
|
May 26, 2026
An exploratory mixed-methods study using the ELICIT framework to identify stakeholder-informed implementation strategies for a population health platform
Anne C Madeo, Jarrod Marable, Polina Kukhareva, et al.
Journal of the American Medical Informatics Association : JAMIA
|
January 12, 2026
GARDE-Chat: a scalable, open-source platform for building and deploying health chatbots
Guilherme Del Fiol, Emerson Borsato, Richard L Bradshaw, et al.
Human Mutation
|
February 11, 2009
Hypo-functional SLC26A4 variants associated with nonsyndromic hearing loss and enlargement of the vestibular aqueduct: genotype-phenotype correlation or coincidental polymorphisms?
Byung Yoon Choi, Andrew K Stewart, Anne C Madeo, et al.
Journal of Medical Genetics
|
September 24, 2011
Allelic hierarchy of CDH23 mutations causing non-syndromic deafness DFNB12 or Usher syndrome USH1D in compound heterozygotes
Julie M Schultz, Rashid Bhatti, Anne C Madeo, et al.
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of 3
Search research articles
Search
Showing results (21-30 of 24) with videos related to
Sort By:
Page
of 3
You have reached the last page of results.
This site can display upto 24 results.
BMC Health Services Research
|
May 26, 2026
An exploratory mixed-methods study using the ELICIT framework to identify stakeholder-informed implementation strategies for a population health platform
Anne C Madeo, Jarrod Marable, Polina Kukhareva, et al.
Journal of the American Medical Informatics Association : JAMIA
|
January 12, 2026
GARDE-Chat: a scalable, open-source platform for building and deploying health chatbots
Guilherme Del Fiol, Emerson Borsato, Richard L Bradshaw, et al.
Human Mutation
|
February 11, 2009
Hypo-functional SLC26A4 variants associated with nonsyndromic hearing loss and enlargement of the vestibular aqueduct: genotype-phenotype correlation or coincidental polymorphisms?
Byung Yoon Choi, Andrew K Stewart, Anne C Madeo, et al.
Journal of Medical Genetics
|
September 24, 2011
Allelic hierarchy of CDH23 mutations causing non-syndromic deafness DFNB12 or Usher syndrome USH1D in compound heterozygotes
Julie M Schultz, Rashid Bhatti, Anne C Madeo, et al.
Page
of 3