Nicholls A.C.,1992

Nicholls A.C., Oliver J., Renouf D.V., Heath D.A., Pope F.M. The molecular defect in a family with mild atypical osteogenesis imperfecta and extreme joint hypermobility: exon skipping caused by an 11-bp deletion from an intron in one COL1A2 allele. - Hum.Genet., 1992, v. 88, p. 627-633.

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