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The American Journal of Dermatopathology
|
May 23, 2009
Human papillomavirus-58 and -73-associated digital squamous cell carcinoma in a patient with aggressive digital papillary adenocarcinoma
William DePond, Kiyoe Kure, Kamani Lankachandra, et al.
Human Genetics
|
June 1, 1991
The clinical phenotype of two patients with a complete deletion of the iduronate-2-sulphatase gene (mucopolysaccharidosis II--Hunter syndrome)
J E Wraith, A Cooper, M Thornley, et al.
Medical Teacher
|
December 12, 2012
Tomorrow's educators … today? Implementing near-peer teaching for medical students
Adam J Nelson, Sophie V Nelson, Andrew M J Linn, et al.
Archives of Physical Medicine and Rehabilitation
|
July 31, 1998
Waddell signs: distributional properties and correlates
D M Novy, H S Collins, D V Nelson, et al.
Ecology and Evolution
|
January 9, 2025
A Genomic-Based Workflow for eDNA Assay Development for a Critically Endangered Turtle, <i>Myuchelys georgesi</i>
Holly V Nelson, Arthur Georges, Katherine A Farquharson, et al.
The Biochemical Journal
|
September 15, 1986
Age-related augmentation of phosphorylase b kinase in hepatic tissue from the glycogen-storage-disease (gsd/gsd) rat
D G Clark, S D Neville, M Brinkman, et al.
BMJ (Clinical Research Ed.)
|
May 25, 1991
Neonatal screening strategy for cystic fibrosis using immunoreactive trypsinogen and direct gene analysis
E Ranieri, R G Ryall, C P Morris, et al.
BMC Health Services Research
|
March 6, 2023
Understanding the Cures Act Information Blocking Rule in cancer care: a mixed methods exploration of patient and clinician perspectives and recommendations for policy makers
Joanna Veazey Brooks, Carli Zegers, Christian T Sinclair, et al.
The Medical Journal of Australia
|
February 18, 1984
Prenatal diagnosis of lysosomal storage diseases. Review of experience in 145 patient referrals over a period of eight years
W F Carey, J J Hopwood, A Poulos, et al.
American Journal of Human Genetics
|
November 1, 1993
Identification of mutations in the alpha-L-iduronidase gene (IDUA) that cause Hurler and Scheie syndromes
H S Scott, T Litjens, P V Nelson, et al.
Page
of 28
Search research articles
Search
Showing results (221-230 of 273) with videos related to
Sort By:
Page
of 28
The American Journal of Dermatopathology
|
May 23, 2009
Human papillomavirus-58 and -73-associated digital squamous cell carcinoma in a patient with aggressive digital papillary adenocarcinoma
William DePond, Kiyoe Kure, Kamani Lankachandra, et al.
Human Genetics
|
June 1, 1991
The clinical phenotype of two patients with a complete deletion of the iduronate-2-sulphatase gene (mucopolysaccharidosis II--Hunter syndrome)
J E Wraith, A Cooper, M Thornley, et al.
Medical Teacher
|
December 12, 2012
Tomorrow's educators … today? Implementing near-peer teaching for medical students
Adam J Nelson, Sophie V Nelson, Andrew M J Linn, et al.
Archives of Physical Medicine and Rehabilitation
|
July 31, 1998
Waddell signs: distributional properties and correlates
D M Novy, H S Collins, D V Nelson, et al.
Ecology and Evolution
|
January 9, 2025
A Genomic-Based Workflow for eDNA Assay Development for a Critically Endangered Turtle, <i>Myuchelys georgesi</i>
Holly V Nelson, Arthur Georges, Katherine A Farquharson, et al.
The Biochemical Journal
|
September 15, 1986
Age-related augmentation of phosphorylase b kinase in hepatic tissue from the glycogen-storage-disease (gsd/gsd) rat
D G Clark, S D Neville, M Brinkman, et al.
BMJ (Clinical Research Ed.)
|
May 25, 1991
Neonatal screening strategy for cystic fibrosis using immunoreactive trypsinogen and direct gene analysis
E Ranieri, R G Ryall, C P Morris, et al.
BMC Health Services Research
|
March 6, 2023
Understanding the Cures Act Information Blocking Rule in cancer care: a mixed methods exploration of patient and clinician perspectives and recommendations for policy makers
Joanna Veazey Brooks, Carli Zegers, Christian T Sinclair, et al.
The Medical Journal of Australia
|
February 18, 1984
Prenatal diagnosis of lysosomal storage diseases. Review of experience in 145 patient referrals over a period of eight years
W F Carey, J J Hopwood, A Poulos, et al.
American Journal of Human Genetics
|
November 1, 1993
Identification of mutations in the alpha-L-iduronidase gene (IDUA) that cause Hurler and Scheie syndromes
H S Scott, T Litjens, P V Nelson, et al.
Page
of 28