Perspectives on the evolution of genetic counselling: Experience over three decades in a family with recurrent lethal osteogenesis imperfecta

Author:

Bascunana C.,El Helou J.,Rauch F.T.,Bardai G.,Glorieux F.H.,Riviere J-B.,Byers P.,Kaplan P.B.,Rosenblatt D.S.

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference8 articles.

1. Lethal osteogenesis imperfecta resulting from a single nucleotide change in one human pro alpha(I) collagen allele;Cohn;Proc. Natl. Acad. Sci. U. S. A.,1986

2. Perinatal lethal osetogenesis imperfecta (OI type II): a biochemically heterogeneious disorder usually due to a new mutation in the genes for type I collagen;Byers;Am. J. Hum. Genet.,1988

3. Recurrence of lethal osteogenesis imperfecta due to parental mosaicism for a dominant mutation in a human type I collagen gene (COL1A1);Cohn;Am. J. Hum. Genet.,1990

4. Recurrence of lethal osteogenesis imperfecta due to parental mosaicism for a mutation in the COL1A2 gene of type I collagen. The mosaic parent exhibits phenotypic features of a mild form of the disease;Edwards;Hum. Mutat.,1992

5. Targeted sequencing of a pediatric metabolic bone gene panel using a desktop semiconductor next-generation sequencer;Rauch;Calcif Tissue Int,2014

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