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BEIGHTON, P [Author]
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Roberts, T S et al.
Rubinstein-Taybi syndrome: Dental manifestations and management
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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
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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
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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
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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
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Orthopaedic manifestations and management
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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
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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
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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
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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
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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
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SAMJ, S. Afr. med. j.
, Mar 2016, vol.106, no.3, p.253-255. ISSN 0256-9574
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