𝔖 Bobbio Scriptorium
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The Phenotype Rhod: Study of Another Family

✍ Scribed by P. Morgan; E. L. Bossom

Book ID
114752941
Publisher
Elsevier Science
Year
1967
Tongue
English
Weight
236 KB
Volume
7
Category
Article
ISSN
0372-1248

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## Abstract Mutations in the genes coding for the proΞ±1 and proΞ±2 chains of type I procollagen have been found in many patients with osteogenesis imperfecta (OI), a heritable disorder of connective tissue. The severity of the disease varies between families and even among members of the same family