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机译:A novel COL1A1 mutation in infantile cortical hyperostosis (Caffey disease) expands the spectrum of collagen-related disorders.
Endocrine and Pediatric Endocrine Units, Department of Medicine, Massachusetts General Hospital and Harvard Medical School, Boston, USA.;
Bone and Bones; Collagen Type I; Hyperostosis; Cortical; Congenital; 骨和骨组织; 骨肥厚; 先天性骨外层;