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Search on : BEIGHTON, P [Author]
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 Roberts, T S et al. Rubinstein-Taybi syndrome: Dental manifestations and management. S. Afr. j. child health, Feb 2014, vol.8, no.1, p.28-30. ISSN 1999-7671
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 Chetty, M et al. UWC - UCT Dental Human Genetics Collaboration: A Report. S. Afr. dent. j., May 2018, vol.73, no.4, p.290-291. ISSN 0011-8516
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 Chetty, M et al. Dental implications of bisphosphonate therapy in osteogenesis imperfecta. S. Afr. dent. j., Oct 2017, vol.72, no.9, p.424-428. ISSN 0011-8516
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 Roberts, T et al. The Tricho-Rhino-Phalangeal syndrome: oral manifestations and management. S. Afr. dent. j., Apr 2014, vol.69, no.4, p.166-169. ISSN 0375-1562
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 Bertie, JD, Beighton, P and Thompson, D The Torg-Winchester form of hereditary osteolysis: Orthopaedic manifestations and management. SA orthop. j., 2013, vol.12, no.2, p.23-27. ISSN 1681-150X
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 Bertie, JD, Thompson, D and Beighton, P Cleidocranial dysplasia presenting as familial coxa vara in a South African family. SA orthop. j., 2011, vol.10, no.2, p.34-38. ISSN 1681-150X
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 Agenbag, G et al. Namaqualand hip dysplasia in South Africa: The molecular determinant elucidated. SAMJ, S. Afr. med. j., Jan 2021, vol.111, no.1, p.57-60. ISSN 0256-9574
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 Vorster, A et al. Osteogenesis imperfecta type 3 in South Africa: Causative mutations in FKBP10. SAMJ, S. Afr. med. j., May 2017, vol.107, no.5, p.457-462. ISSN 0256-9574
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 Spencer, C et al. A clinical and molecular investigation of two South African families with Simpson-Golabi-Behmel syndrome. SAMJ, S. Afr. med. j., Mar 2016, vol.106, no.3, p.272-275. ISSN 0256-9574
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 Vorster, A A, Beighton, P and Ramesar, R S Digitotalar dysmorphism: Molecular elucidation. SAMJ, S. Afr. med. j., Mar 2016, vol.106, no.3, p.253-255. ISSN 0256-9574
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