Found: 15
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Physical Activity and Quality of Life in People With Visual Impairments: A Systematic Review.
- Published in:
- Journal of Visual Impairment & Blindness, 2022, v. 116, n. 1, p. 48, doi. 10.1177/0145482X211072567
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- Article
Response to sodium benzoate treatment in non-ketotic hyperglycinaemia.
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- Pediatrics International, 1994, v. 36, n. 1, p. 75, doi. 10.1111/j.1442-200X.1994.tb03134.x
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- Article
A morphoscopic exploration of cranial sexual dimorphism among modern South Africans using computed tomography scans.
- Published in:
- International Journal of Legal Medicine, 2024, v. 138, n. 6, p. 2635, doi. 10.1007/s00414-024-03283-3
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- Article
Postcraniometric sex and ancestry estimation in South Africa: a validation study.
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- International Journal of Legal Medicine, 2019, v. 133, n. 1, p. 289, doi. 10.1007/s00414-018-1865-x
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- Article
Sex estimation from the long bones of modern South Africans.
- Published in:
- International Journal of Legal Medicine, 2017, v. 131, n. 1, p. 275, doi. 10.1007/s00414-016-1488-z
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- Article
Erratum to: Sexual dimorphism in cranial morphology among modern South Africans.
- Published in:
- 2015
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- Publication type:
- Erratum
Sexual dimorphism in cranial morphology among modern South Africans.
- Published in:
- International Journal of Legal Medicine, 2015, v. 129, n. 4, p. 869, doi. 10.1007/s00414-014-1111-0
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- Publication type:
- Article
Multiple giant cell lesions in patients with Noonan syndrome and cardio-facio-cutaneous syndrome.
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- European Journal of Human Genetics, 2009, v. 17, n. 4, p. 420, doi. 10.1038/ejhg.2008.188
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- Article
Testing the parents to confirm genotypes of CF patients is highly recommended: report of two cases.
- Published in:
- European Journal of Human Genetics, 2009, v. 17, n. 4, p. 417, doi. 10.1038/ejhg.2008.190
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- Publication type:
- Article
Deletions in the 3′ Part of the NFIX Gene Including a Recurrent Alu-Mediated Deletion of Exon 6 and 7 Account for Previously Unexplained Cases of Marshall- Smith Syndrome.
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- Human Mutation, 2014, v. 35, n. 9, p. 1092, doi. 10.1002/humu.22603
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- Article
Intronic mutations in the L1CAM gene may cause X-linked hydrocephalus by aberrant splicing.
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- Human Mutation, 2004, v. 23, n. 5, p. 526, doi. 10.1002/humu.9242
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- Article
Veldt fires in South Africa: Implications on osteometry and the biological profile.
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- Journal of Forensic Sciences, 2023, v. 68, n. 2, p. 586, doi. 10.1111/1556-4029.15194
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- Publication type:
- Article
Long-term follow-up in females with Ullrich-Turner syndrome.
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- Clinical Genetics, 1991, v. 40, n. 1, p. 1, doi. 10.1111/j.1399-0004.1991.tb03061.x
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- Article
Isochromosome (18q) in siblings.
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- Clinical Genetics, 1987, v. 32, n. 4, p. 249, doi. 10.1111/j.1399-0004.1987.tb03308.x
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- Publication type:
- Article
Expanded spectrum of exon 33 and 34 mutations in SRCAP and follow-up in patients with Floating-Harbor syndrome
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- BMC Medical Genetics, 2014, v. 15, n. 1, p. 127, doi. 10.1186/s12881-014-0127-0
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- Publication type:
- Article