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European Journal of Human Genetics : EJHG|November 30, 2022
LARS2 variants can present as premature ovarian insufficiency in the absence of overt hearing lossAnne Sophie Neyroud, Joëlle Rudinger-Thirion, Magali Frugier, et al.
Molecular Genetics and Metabolism|December 19, 2018
Cryptic intronic NBAS variant reveals the genetic basis of recurrent liver failure in a childRocio Rius, Lisa G Riley, Yiran Guo, et al.
Frontiers in Genetics|August 22, 2022
DNA methylation patterns and gene expression from amygdala tissue of mature Brahman cows exposed to prenatal stressEmilie C Baker, Audrey L Earnhardt, Kubra Z Cilkiz, et al.
Journal of Economic Entomology|November 19, 2025
Leaf trichome and insecticide interactions relative to Bemisia tabaci (Hemiptera: Aleyrodidae) management in a cotton-cucurbit strip cropping arrangementPaulo S G Cremonez, Arash Kheirodin, Jermaine D Perier, et al.
JIMD Reports|November 6, 2015
LARS2 Variants Associated with Hydrops, Lactic Acidosis, Sideroblastic Anemia, and Multisystem FailureLisa G Riley, Joëlle Rudinger-Thirion, Klaus Schmitz-Abe, et al.
European Journal of Human Genetics : EJHG|May 30, 2024
Genome sequencing enables diagnosis and treatment of SLC5A6 neuropathyLisa G Riley, Subrata Sabui, Hamid M Said, et al.
Neurology. Genetics|January 26, 2023
Expanding the Allelic Heterogeneity of ANO10-Associated Autosomal Recessive Cerebellar AtaxiaSean Massey, Yiran Guo, Lisa G Riley, et al.
Blood Advances|April 27, 2022
Functional interaction between compound heterozygous TERT mutations causes severe telomere biology disorderAram Niaz, Jia Truong, Annabel Manoleras, et al.
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