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.
Смотрите также:
