Search research articles
Contact Us
Filters
Showing results (231-240 of 233) with videos related to
Page
of 24
Sort By:
You have reached the last page of results.
This site can display upto 233 results.
JAMA Ophthalmology
|
December 4, 2025
Early-Onset Retinopathy in Patients With Variants in SLC6A6 Leading to Impaired Taurine Transport
Mukhtar Ullah, Atta Ur Rehman, Madhur Shetty, et al.
Annals of the Rheumatic Diseases
|
July 22, 2022
Gain-of-function mutations in <i>ALPK1</i> cause an NF-κB-mediated autoinflammatory disease: functional assessment, clinical phenotyping and disease course of patients with ROSAH syndrome
Christina Torres Kozycki, Shilpa Kodati, Laryssa Huryn, et al.
Medrxiv : the Preprint Server for Health Sciences
|
July 3, 2026
Structural variant discovery and diagnostic impact in rare diseases from short-read and long-read sequencing
Alba Sanchis-Juan, Yulia Mostovoy, Sarah L Stenton, et al.
Page
of 24
Search research articles
Search
Showing results (231-240 of 233) with videos related to
Sort By:
Page
of 24
You have reached the last page of results.
This site can display upto 233 results.
JAMA Ophthalmology
|
December 4, 2025
Early-Onset Retinopathy in Patients With Variants in SLC6A6 Leading to Impaired Taurine Transport
Mukhtar Ullah, Atta Ur Rehman, Madhur Shetty, et al.
Annals of the Rheumatic Diseases
|
July 22, 2022
Gain-of-function mutations in <i>ALPK1</i> cause an NF-κB-mediated autoinflammatory disease: functional assessment, clinical phenotyping and disease course of patients with ROSAH syndrome
Christina Torres Kozycki, Shilpa Kodati, Laryssa Huryn, et al.
Medrxiv : the Preprint Server for Health Sciences
|
July 3, 2026
Structural variant discovery and diagnostic impact in rare diseases from short-read and long-read sequencing
Alba Sanchis-Juan, Yulia Mostovoy, Sarah L Stenton, et al.
Page
of 24