Works matching IS 00034800 AND DT 2025 AND VI 89 AND IP 1
Results: 7
Gastroesophageal reflux disease increases predisposition to severe COVID‐19: Insights from integrated Mendelian randomization and genetic analysis.
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- Annals of Human Genetics, 2025, v. 89, n. 1, p. 54, doi. 10.1111/ahg.12584
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- Article
Clinical and immunological features of four patients with activation‐induced cytidine deaminase deficiency: Renal amyloidosis and other presentations.
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- Annals of Human Genetics, 2025, v. 89, n. 1, p. 47, doi. 10.1111/ahg.12583
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- Article
DYNC2H1 splicing variants causing severe prenatal short‐rib polydactyly syndrome and postnatal orofaciodigital syndrome.
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- Annals of Human Genetics, 2025, v. 89, n. 1, p. 24, doi. 10.1111/ahg.12581
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- Article
Traces of Bronze Age globalization in East Asia: Insights from a revised phylogeography of the Y‐chromosome haplogroup Q1a1a‐M120.
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- Annals of Human Genetics, 2025, v. 89, n. 1, p. 12, doi. 10.1111/ahg.12580
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- Article
Genetic analyses of a large consanguineous south Indian family reveal novel variants in NAGPA and four hitherto unreported genes in developmental stuttering.
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- Annals of Human Genetics, 2025, v. 89, n. 1, p. 31, doi. 10.1111/ahg.12579
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- Article
Heritability and genetic correlations of obesity indices and cardiometabolic traits in the Northern Chinese families.
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- Annals of Human Genetics, 2025, v. 89, n. 1, p. 1, doi. 10.1111/ahg.12578
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- Article
Issue Information.
- Published in:
- Annals of Human Genetics, 2025, v. 89, n. 1, p. 1, doi. 10.1111/ahg.12565
- Publication type:
- Article