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Complete Structure of the Human COL11A2 Gene: The Exon Sizes and other Features Indicate the Gene Has Not Evolved with Genes for Other Fibriller Collagens.
- Published in:
- Annals of the New York Academy of Sciences, 1996, v. 785, n. 1, p. 343, doi. 10.1111/j.1749-6632.1996.tb56304.x
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- Article
Novel patients with NHLRC2 variants expand the phenotypic spectrum of FINCA disease.
- Published in:
- Frontiers in Neuroscience, 2023, p. 01, doi. 10.3389/fnins.2023.1123327
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- Article
Consortium for osteogenesis imperfecta mutations in the helical domain of type I collagen: regions rich in lethal mutations align with collagen binding sites for integrins and proteoglycans.
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- Human Mutation, 2007, v. 28, n. 3, p. 209, doi. 10.1002/humu.20429
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- Article
Lack of correlation between the type of COL1A1 or COL1A2 mutation and hearing loss in osteogenesis imperfecta patients.
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- Human Mutation, 2004, v. 24, n. 5, p. 437, doi. 10.1002/humu.20108
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- Article
Lack of correlation between the type of COL1A1 or COL1A2 mutation and hearing loss in osteogenesis imperfecta patients.
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- Human Mutation, 2004, v. 24, n. 2, p. 147, doi. 10.1002/humu.20071
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- Article
Use of conformation sensitive gel electrophoresis to detect single-base changes in the gene for COL10A1.
- Published in:
- Human Mutation, 1998, v. 11, p. S201, doi. 10.1002/humu.1380110165
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- Article
Two new recurrent nucleotide mutations in the COL1A1 gene in four patients with osteogenesis imperfecta: About one-fifth are recurrent.
- Published in:
- Human Mutation, 1997, v. 9, n. 2, p. 148, doi. 10.1002/(SICI)1098-1004(1997)9:2<148::AID-HUMU7>3.0.CO;2-5
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- Article