DOI:
10.1055/s-00029027
Journal of Pediatric Genetics
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References
Faqeih E, Roughley P, Glorieux FH, Rauch F.
Osteogenesis imperfecta type III with intracranial hemorrhage and brachydactyly associated with mutations in exon 49 of COL1A2.
Am J Med Genet A 2009;
149A (03) 461-465
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