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Frontiers in Genetics|April 14, 2023
Case Report: Identification of a rare nonsense mutation in the POC1A gene by NGS in a diabetes mellitus patientDongfeng Li, Shihui Li, Jingjing Zhou, et al.
Frontiers in Genetics|April 14, 2023
Genotype-phenotype pattern analysis of pathogenic PAX9 variants in Chinese Han families with non-syndromic oligodontiaJiabao Ren, Sifang Gan, Shushen Zheng, et al.
Frontiers in Genetics|April 7, 2023
Case report: Homozygous variants of NEB and KLHL40 in two Arab patients with nemaline myopathyCristina Skrypnyk, Aseel Ahmed Husain, Hisham Y Hassan, et al.
Frontiers in Genetics|April 7, 2023
Distribution of a novel CYP2C haplotype in Native American populationsVanessa Câmara Fernandes, Marco Antônio M Pretti, Luiza Tamie Tsuneto, et al.
Frontiers in Genetics|April 7, 2023
A novel SETD2 variant causing global development delay without overgrowth in a Chinese 3-year-old boyYuanyuan Wu, Fang Liu, Ruihua Wan, et al.
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