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PNPT1, MYO15A, PTPRQ, and SLC12A2‐associated genetic and phenotypic heterogeneity among hearing impaired assortative mating families in Southern India.
- Published in:
- Annals of Human Genetics, 2022, v. 86, n. 1, p. 1, doi. 10.1111/ahg.12442
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- Article
Issue Information.
- Published in:
- Annals of Human Genetics, 2022, v. 86, n. 1, p. i, doi. 10.1111/ahg.12430
- Publication type:
- Article
Clinical features of patients with Yin Yang 1 deficiency causing Gabriele‐de Vries syndrome: A new case and review of the literature.
- Published in:
- Annals of Human Genetics, 2022, v. 86, n. 1, p. 52, doi. 10.1111/ahg.12448
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- Article
Tools for standardized data collection: Speech, Language, and Hearing measurement protocols in the PhenX Toolkit.
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- Annals of Human Genetics, 2022, v. 86, n. 1, p. 45, doi. 10.1111/ahg.12447
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- Article
Genetics of ataxia telangiectasia in a highly consanguineous population.
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- Annals of Human Genetics, 2022, v. 86, n. 1, p. 34, doi. 10.1111/ahg.12445
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- Article
The hazards of genotype imputation in chromosomal regions under selection: A case study using the Lactase gene region.
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- Annals of Human Genetics, 2022, v. 86, n. 1, p. 24, doi. 10.1111/ahg.12444
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- Publication type:
- Article
Interaction between the genetic variant of rs696217‐ghrelin and food intake and obesity and dyslipidemia.
- Published in:
- Annals of Human Genetics, 2022, v. 86, n. 1, p. 14, doi. 10.1111/ahg.12443
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- Article