A cross-sectional multicenter study of osteogenesis imperfecta in North America - results from the linked clinical research centers-Reference-Cited by-同舟云学术

A cross-sectional multicenter study of osteogenesis imperfecta in North America - results from the linked clinical research centers

Published:2014-05-30 Issue:2 Volume:87 Page:133-140
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:Clin Genet

Author:

Patel R.M.¹,Nagamani S.C.S.¹,Cuthbertson D.²,Campeau P.M.¹,Krischer J.P.²,Shapiro J.R.³,Steiner R.D.⁴⁵,Smith P.A.⁶,Bober M.B.⁷,Byers P.H.⁸,Pepin M.⁸,Durigova M.⁹,Glorieux F.H.⁹,Rauch F.⁹,Lee B.H.¹¹⁰,Hart T.¹¹,Sutton V.R.¹

Affiliation:

1. Department of Molecular and Human Genetics; Baylor College of Medicine; Houston TX USA

2. College of Medicine; University of South Florida; Tampa FL USA

3. Department of Bone and Osteogenesis Imperfecta; Kennedy Krieger Institute; Baltimore MD USA

4. Departments of Pediatrics and Molecular and Medical Genetics; Oregon Health & Science University; Portland OR USA

5. Marshfield Clinic Research Foundation; University of Wisconsin; Marshfield WI USA

6. Department of Orthopaedic Surgery; Shriners Hospitals for Children; Chicago IL USA

7. Division of Medical Genetics; Alfred I. duPont Hospital for Children; Wilmington DE USA

8. Departments of Medicine and Pathology, Division of Medical Genetics; University of Washington; Seattle WA USA

9. Department of Orthopaedic Surgery; Shriners Hospital for Children and McGill University; Montreal QC Canada

10. Department of Molecular and Human Genetics; Howard Hughes Medical Institute; Houston TX USA

11. Osteogenesis Imperfecta Foundation; Gaithersburg MD USA

Funder

Osteogenesis Imperfecta Foundation

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference47 articles.

1. Osteogenesis imperfecta;Rauch;Lancet,2004

2. Genetic heterogeneity in osteogenesis imperfecta;Sillence;J Med Genet,1979

3. Osteogenesis imperfecta is linked to both type I collagen structural genes;Sykes;Lancet,1986

4. CRTAP is required for prolyl 3- hydroxylation and mutations cause recessive osteogenesis imperfecta;Morello;Cell,2006

5. Deficiency of cartilage-associated protein in recessive lethal osteogenesis imperfecta;Barnes;N Engl J Med,2006

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