Tetralogy of fallot in a patient with developmental coxa vara/spondylometaphyseal dysplasia-corner fracture type (DCV/SMD-CF) expanding the variability
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Reference14 articles.
1. Recessive Robinow syndrome, allelic to dominant brachydactyly type B, is caused by mutation of ROR2;Afzal;Nat Genet,2000
2. Metaphyseal dysostosis: Description of an ultrastructure defect in epiphyseal plate chondrocytes. Case report;Cooper;J Bone Joint Surg Am,1973
3. Developmental coxa vara associated with spondylometaphyseal dysplasia (DCV/SMD): “SMD-corner Fracture Type” (DCV/SMD-CF) demostrated in most reported cases;Currarino;Pediatr Radiol,2000
4. Spondylometaphyseal dysplasia: A variant form;Felman;Radiology,1974
5. Spondylo-metaphyseal dysplasia Sutcliffe type;Kozlowski;Br J Radiol,1989
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1. Unexpected findings in cervical spine in spondylometaphyseal dysplasia Sutcliff type FN1‐related;American Journal of Medical Genetics Part A;2023-11-08
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