Screening for congenital dislocation of the hip in AustraliaCOLE, W. G.Journal of paediatrics and child health. 1991, Vol 27, Num 3, pp 143-146, issn 1034-4810Article

Collagen genes: mutations affecting collagen structure and expressionCOLE, W. G.Progress in nucleic acid research and molecular biology. 1994, Vol 47, pp 29-80, issn 0079-6603Article

Treatment of early-acute osteomyelitis in childhood: brief reportCOLE, W. G.Journal of bone and joint surgery. British volume. 1987, Vol 69, Num 5, pp 845-846, issn 0301-620XArticle

Early surgical management of severe forms of osteogenesis imperfectaCOLE, W. G.American journal of medical genetics. 1993, Vol 45, Num 2, pp 270-274, issn 0148-7299Conference Paper

Abnormal skeletal growth in Kniest dysplasia caused by Type II collagen mutationsCOLE, W. G.Clinical orthopaedics and related research. 1997, Num 341, pp 162-169, issn 0009-921XArticle

Etiology and pathogenesis of heritable connective tissue diseasesCOLE, W. G.Journal of pediatric orthopedics. 1993, Vol 13, Num 3, pp 392-403, issn 0271-6798Article

The management of chronic osteomyelitisCOLE, W. G.Clinical orthopaedics and related research. 1991, Num 264, pp 84-89, issn 0009-921XArticle

Treatment of aneurysmal bone cysts in childhoodCOLE, W. G.Journal of pediatric orthopedics. 1986, Vol 6, Num 3, pp 326-329, issn 0271-6798Article

Genetics of connective tissue diseaseCOLE, W. G.Medical journal of Australia. 1993, Vol 158, Num 10, pp 678-680, issn 0025-729XArticle

Three graphic representations to aid Bayesian inferenceCOLE, W. G.Methods of information in medicine. 1988, Vol 27, Num 3, pp 125-132, issn 0026-1270Article

The Nicholas Andry Award-1996: The molecular pathology of osteogenesis imperfectaCOLE, W. G.Clinical orthopaedics and related research. 1997, Num 343, pp 235-248, issn 0009-921XArticle

Perinatal lethal osteogenesis imperfectaCOLE, W. G; DALGLEISH, R.Journal of medical genetics. 1995, Vol 32, Num 4, pp 284-289, issn 0022-2593Article

Quantitation of type I and III collagens using electrophoresis of alpha chains and cyanogen bromide peptidesCHAN, D; COLE, W. G.Analytical biochemistry. 1984, Vol 139, Num 2, pp 322-328, issn 0003-2697Article

Low basal transcription of genes for tissue-specific collagens by fibroblasts and lymphoblastoid cells : application to the characterization of a glycine 997 to serine substitution in α1(II) collagen chains of a patient with spondylepiphyseal dysplasiaCHAN, D; COLE, W. G.The Journal of biological chemistry (Print). 1991, Vol 266, Num 19, pp 12487-12494, issn 0021-9258Article

Early plaster treatment for fractures of the femoral shaft in childhoodSUGI, M; COLE, W. G.Journal of bone and joint surgery. British volume. 1987, Vol 69, Num 5, pp 743-745, issn 0301-620XArticle

Alternative splicing of exon 37 of FBN1 deletes part of an 'eight-cysteine' domain resulting in the Marfan syndromeMCGRORY, J; COLE, W. G.Clinical genetics. 1999, Vol 55, Num 2, pp 118-121, issn 0009-9163Article

Novel mutations affecting LRP5 splicing in patients with osteoporosis-pseudoglioma syndrome (OPPG)LAINE, C. M; CHUNG, B. D; COLE, W. G et al.European journal of human genetics. 2011, Vol 19, Num 8, pp 875-881, issn 1018-4813, 7 p.Article

Missense mutations in the β strands of the single A-domain of matrilin-3 result in multiple epiphyseal dysplasiaJACKSON, G. C; BARKER, F. S; MORTIER, G. R et al.Journal of medical genetics. 2004, Vol 41, Num 1, pp 52-59, issn 0022-2593, 8 p.Article

Age characteristics of coarse woody debris (Pinus strobus) in a lake littoral zoneGUYETTE, R. P; COLE, W. G.Canadian journal of fisheries and aquatic sciences (Print). 1999, Vol 56, Num 3, pp 496-505, issn 0706-652XArticle

Management of subtrochanteric fractures of the femur in childrenTHEOLOGIS, T. N; COLE, W. G.Journal of pediatric orthopedics. 1998, Vol 18, Num 1, pp 22-25, issn 0271-6798Article

Mutation analysis of LMX1B gene in nail-patella syndrome patientsMCINTOSH, L; DREYER, S. D; ZABEL, B et al.American journal of human genetics. 1998, Vol 63, Num 6, pp 1651-1658, issn 0002-9297Article

Constitutively activated receptors for parathyroid hormone and parathyroid hormone-related peptide in Jansen's metaphyseal chondrodysplasiaSCHIPANI, E; LANGMAN, C. B; PARFITT, A. M et al.The New England journal of medicine. 1996, Vol 335, Num 10, pp 708-714, issn 0028-4793Article

Pes anserinus syndrome due to solitary tibial spurs and osteochondromasFRASER, R. K; NATTRASS, G. R; CHOW, C. W et al.Journal of pediatric orthopedics. 1996, Vol 16, Num 2, pp 247-248, issn 0271-6798Article

The clinical features of spondyloepiphyseal dysplasia congenita resulting from the substitution of glycine 997 by serine in the α1(II) chain of type II collagenCOLE, W. G; HALL, R. K; ROGERS, J. G et al.Journal of medical genetics. 1993, Vol 30, Num 1, pp 27-35, issn 0022-2593Article

The paediatric cervical seat belt syndromeHOY, G. A; COLE, W. G.Injury. 1993, Vol 24, Num 5, pp 297-299, issn 0020-1383Article