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A new culprit in osteogenesis imperfecta

✍ Scribed by Emily L Germain-Lee

Publisher
American Society for Bone and Mineral Research
Year
2011
Tongue
English
Weight
61 KB
Volume
26
Category
Article
ISSN
0884-0431

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The only serious attempts at linkage in osteogenesis imperfecta (01) have shown that the disease is linked to type 1 collagen genes in all families studied in which it segregrates as a clear mendelian dominant trait. For prenatal diagnosis the probability that a new family is linked can be taken as

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The objective of this study was to examine whether parental age is associated with the occurrence of apparently sporadic osteogenesis imperfecta (OI). We compared parental age and the joint distribution of maternal and paternal age with expected distributions based on statutory birth records for eac