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Pediatric Neurology|June 20, 2026
Epidemiologic, Clinical, and Molecular Landscape of Neurofibromatosis Type 1 in Oman: A Study of 211 IndividualsHoor K Al Nabhani, Fatema M Al Shamsi, Safa S Al Shuaili, et al.Research Square|November 1, 2024
Genotype-phenotype correlation in recessive DNAJB4 myopathyMichio Inoue, Divya Jayaraman, Rocio Bengoechea, et al.Acta Neuropathologica Communications|October 29, 2024
Genotype‒phenotype correlation in recessive DNAJB4 myopathyMichio Inoue, Divya Jayaraman, Rocio Bengoechea, et al.Journal of Community Genetics|February 18, 2022
Uptake of prenatal genetic diagnosis and termination of pregnancy by Omani Muslim families at risk of genetic disorders: experience over a 9-year periodZandré Bruwer, Salwa Al Ubaidani, Khalsa Al Kharusi, et al.The Journal of Allergy and Clinical Immunology|March 4, 2021
Loss of DIAPH1 causes SCBMS, combined immunodeficiency, and mitochondrial dysfunctionMeri Kaustio, Naemeh Nayebzadeh, Reetta Hinttala, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 20, 2021
Combining exome/genome sequencing with data repository analysis reveals novel gene-disease associations for a wide range of genetic disordersAida M Bertoli-Avella, Krishna K Kandaswamy, Suliman Khan, et al.Pageof 3