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The Journal of Clinical Investigation
|
December 26, 2001
A mutation in the human MPDU1 gene causes congenital disorder of glycosylation type If (CDG-If)
C Kranz, J Denecke, M A Lehrman, et al.
Pediatric Research
|
March 27, 2001
Normal clinical outcome in untreated subjects with mild hyperphenylalaninemia
J Weglage, M Pietsch, R Feldmann, et al.
AJNR. American Journal of Neuroradiology
|
June 30, 2022
Brain Abnormalities in Patients with Germline Variants in <i>H3F3</i>: Novel Imaging Findings and Neurologic Symptoms Beyond Somatic Variants and Brain Tumors
C A P F Alves, O Sherbini, F D'Arco, et al.
Page
of 4
Search research articles
Search
Showing results (31-40 of 33) with videos related to
Sort By:
Page
of 4
You have reached the last page of results.
This site can display upto 33 results.
The Journal of Clinical Investigation
|
December 26, 2001
A mutation in the human MPDU1 gene causes congenital disorder of glycosylation type If (CDG-If)
C Kranz, J Denecke, M A Lehrman, et al.
Pediatric Research
|
March 27, 2001
Normal clinical outcome in untreated subjects with mild hyperphenylalaninemia
J Weglage, M Pietsch, R Feldmann, et al.
AJNR. American Journal of Neuroradiology
|
June 30, 2022
Brain Abnormalities in Patients with Germline Variants in <i>H3F3</i>: Novel Imaging Findings and Neurologic Symptoms Beyond Somatic Variants and Brain Tumors
C A P F Alves, O Sherbini, F D'Arco, et al.
Page
of 4