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Tian Cheng Department of Clinical Science, Intervention and Technology (CLINTEC), Karolinska Institutet, Stockholm, Sweden

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Elisabet Einarsdottir Department of Gene Technology, School of Engineering Sciences in Chemistry, Biotechnology and Health, Royal Institute of Technology, Stockholm, Sweden

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Juha Kere Department of Biosciences and Nutrition (BioNut), Karolinska Institutet, Stockholm, Sweden
Folkhälsan Research Center, Helsinki, Finland

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Paul Gerdhem Department of Clinical Science, Intervention and Technology (CLINTEC), Karolinska Institutet, Stockholm, Sweden
Department of Reconstructive Orthopaedics, Karolinska University Hospital, Stockholm, Sweden

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contribute to the phenotype of scoliosis are unclear. Furthermore, the currently well-known and replicated loci can only explain a small percentage of all possible loci and the missing heritability remains a concern ( 14 , 15 , 16 , 17 , 18 , 19 , 20

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Shankar Aissvarya Department of Biomedical Sciences, Faculty of Medicine and Health Sciences, Universiti Putra Malaysia, Serdang, Selangor, Malaysia

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King-Hwa Ling Department of Biomedical Sciences, Faculty of Medicine and Health Sciences, Universiti Putra Malaysia, Serdang, Selangor, Malaysia
Genetics & Regenerative Medicine Research Group, Faculty of Medicine and Health Sciences, Universiti Putra Malaysia, Serdang, Selangor, Malaysia
Malaysian Research Institute on Ageing (MyAgeing), Universiti Putra Malaysia, Serdang, Selangor, Malaysia

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Manohar Arumugam Department of Orthopaedics, Faculty of Medicine and Health Sciences, Universiti Putra Malaysia, Serdang, Selangor, Malaysia
School of Medicine, Faculty of Medicine and Health Sciences, Taylor's University, Selangor, Malaysia

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Karuppiah Thilakavathy Department of Biomedical Sciences, Faculty of Medicine and Health Sciences, Universiti Putra Malaysia, Serdang, Selangor, Malaysia
Genetics & Regenerative Medicine Research Group, Faculty of Medicine and Health Sciences, Universiti Putra Malaysia, Serdang, Selangor, Malaysia
Malaysian Research Institute on Ageing (MyAgeing), Universiti Putra Malaysia, Serdang, Selangor, Malaysia

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cytogenetic aberrations on chromosomes 5 and 11 for DC ( 24 ). Familial and twin studies Twin studies make a useful tool in identifying genetic influences in the heritability of a disease. In a comparative study of two pairs of twins, it was observed

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Ioannis Gkiatas Orthopaedic Department, School of Medicine, University of Ioannina, Ioannina, Greece

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Anastasia Boptsi Orthopaedic Department, School of Medicine, University of Ioannina, Ioannina, Greece

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Dimitra Tserga Orthopaedic Department, School of Medicine, University of Ioannina, Ioannina, Greece

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Ioannis Gelalis Orthopaedic Department, School of Medicine, University of Ioannina, Ioannina, Greece

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Dimitrios Kosmas Orthopaedic Department, School of Medicine, University of Ioannina, Ioannina, Greece

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Emilios Pakos Orthopaedic Department, School of Medicine, University of Ioannina, Ioannina, Greece

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According to a single-centre study hip dysplasia is associated with osteogenesis imperfecta (OI), a heritable skeletal disorder that is usually due to mutation in one of the two genes, COL1A1 and COL1A2, that code for collagen type I a-chains. This study

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Rita Grazina Serviço de Ortopedia e Traumatologia, Centro Hospitalar Vila Nova de Gaia/Espinho, Portugal

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Sérgio Teixeira Serviço de Cirurgia Plástica, Reconstrutiva e Estética e Unidade de Queimados, Centro Hospitalar de São João, Portugal

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Renato Ramos Serviço de Ortopedia e Traumatologia, Centro Hospitalar Vila Nova de Gaia/Espinho, Portugal

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Henrique Sousa Serviço de Ortopedia e Traumatologia, Centro Hospitalar Vila Nova de Gaia/Espinho, Portugal

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Andreia Ferreira Serviço de Ortopedia e Traumatologia, Centro Hospitalar Vila Nova de Gaia/Espinho, Portugal

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Rui Lemos Serviço de Ortopedia e Traumatologia, Centro Hospitalar Vila Nova de Gaia/Espinho, Portugal

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. The heritability of Dupuytren’s disease: familial aggregation and its clinical significance . J Hand Surg Am 2006 ; 31 : 204 - 210 . 15. Larsen S Krogsgaard DG Larsen LA . Genetic and environmental influences in

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T Gosens Department of Orthopedic and Trauma Surgery, Elisabeth-TweeSteden Hospital, Tilburg, The Netherlands
Department of Medical and Clinical Psychology, Tilburg University, Tilburg, The Netherlands
Center of Research on Psychological and Somatic disorders (CoRPS), Tilburg University, Tilburg, The Netherlands

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B L den Oudsten Department of Medical and Clinical Psychology, Tilburg University, Tilburg, The Netherlands
Center of Research on Psychological and Somatic disorders (CoRPS), Tilburg University, Tilburg, The Netherlands

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outcome ( 46 ). As a trait, resilience refers to a characteristic of personality, which is heritable and relatively stable across time ( 47 ). The American Psychological Association defines resilience as ‘the process and outcome of successfully adapting to

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Alpesh Kothari Department of Paediatric Orthopaedics, Oxford University Hospitals NHS Foundation Trust, Oxford, United Kingdom

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Javier Masquijo Department of Pediatric Orthopaedics, Sanatorio Allende, Córdoba, Argentina

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true incidence of tarsal coalition is unknown, estimates vary from 1% to 13%, 1 , 2 thereby making it one of the commonest foot and ankle pathologies in children. Coalitions are bilateral in approximately 50% of cases, and there is a heritable

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Mariam S Alharbi Internal Medicine Department, College of Medicine, Qassim University, Buraydah, Saudi Arabia

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, National Library of Medicine , 2000 .( https://doi.org/10.1002/(SICI)1098-1004(200001)15:1<57::AID-HUMU12>3.0.CO;2-G ) 30 White CB The mucopolysaccharidoses . In McKusick’s Heritable Disorders of Connective Tissue , pp. 367 – 350 . Ed Beighton P

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