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Global Medical Genetics|November 29, 2023
The Epigenetic Regulation of Quiescent in Stem CellsMehran Radak, Hossein Fallahi
Global Medical Genetics|November 29, 2023
Severe Hypernatremia as Presentation of Netherton SyndromeA Di Nora, M C Consentino, G Messina, et al.
Global Medical Genetics|May 11, 2026
DNA methylation and exosomes in relation to type 2 diabetes in Black South Africans: A pilot studyBuhle B Mbali, Laverdure T Piame, Sesethu Sehole, et al.
Global Medical Genetics|February 25, 2026
Pediatric toe-walking cohort with heterozygous SBF1 variants: A phenotypic descriptionDavid Pomarino, Amel Sidi Athmane, Bastian Fregien, et al.
Global Medical Genetics|April 10, 2026
Molecular mechanism study of novel compound heterozygous EOGT mutations leading to Adams-Oliver syndrome type 4Yufei He, Xiangyu Liu, Zongrui Shen, et al.
Global Medical Genetics|October 12, 2023
Imaging in a Rare Case of Neonatal Arterial Tortuosity SyndromeMaria Cristina Inserra, Alessia Di Mari, Giulia Passaniti, et al.
Global Medical Genetics|July 17, 2023
BL-MOL-AR Project, Preliminary Results about Liquid Biopsy: Molecular Approach Experience and Research Activity in Oncological SettingsAlessandro Pancrazzi, Francesco Bloise, Alice Moncada, et al.
Global Medical Genetics|July 28, 2023
Molecular Evaluation of Joubert Syndrome and Hearing Impairment in a Patient with Ataxic Cerebral PalsyN Sreedevi, N Swapna, Santosh Maruthy, et al.
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