Articular degeneration as a sequela of osteochondrodysplasiasSTANESCU, V; STANESCU, R; MAROTEAUX, P et al.Clinics in rheumatic diseases. 1985, Vol 11, Num 2, pp 239-270, issn 0307-742XArticle

Pathogenic mechanisms in osteochondrodysplasiasSTANESCU, V; STANESCU, R; MAROTEAUX, P et al.Journal of bone and joint surgery. American volume. 1984, Vol 66, Num 6, pp 817-836, issn 0021-9355Article

The absence of type II collagen and changes in proteoglycan structure of hyaline cartilage in a case of Langer-Saldino achondrogenesisFESHCHENKO, S. P; REBRIN, I. A; SOKOLNIK, V. P et al.Human genetics. 1989, Vol 82, Num 1, pp 49-54, issn 0340-6717, 6 p.Article

The birth prevalence rates for the skeletal dysplasiasORIOLI, I. M; CASTILLA, E. E; BARBOSA-NETO, J. G et al.Journal of medical genetics. 1986, Vol 23, Num 4, pp 328-332, issn 0022-2593Article

Pathologic changes of osteochondrodysplasia in infancy: a reviewGILBERT, E. F; YANG, S. S; LANGER, L et al.Pathology annual. 1987, Vol 22, Num 2, pp 283-345, issn 0079-0184Article

Histopathologic examination in osteochondrodysplasia. Time for standardizationYANG, S. S; KITCHEN, E; GILBERT, E. F et al.Archives of pathology & laboratory medicine (1976). 1986, Vol 110, Num 1, pp 10-12, issn 0363-0153Article

The infrequency of malignant disease in diapheseal aclasis and neurofibromatosisVOUTSINAS, S; WYNNE-DAVIES, R.Journal of medical genetics. 1983, Vol 20, Num 5, pp 345-349, issn 0022-2593Article

Achondrogenesis: new nosology with evidence of genetic heterogeneityWHITLEY, C. B; GORLIN, R. J.Radiology. 1983, Vol 148, Num 3, pp 693-698, issn 0033-8419Article

A distinct chondrodysplasia resembling Kniest dysplasia: clinical, roentgenographic, histologic, and ultrastructural findingsSCONYERS, S. M; RIMOIN, D. L; LACHMAN, R. S et al.The Journal of pediatrics. 1983, Vol 103, Num 6, pp 898-904, issn 0022-3476Article

Dysplasies et dystrophies osseuses. Le point de vue de l'anatomopathologiste = Bone dysplasia and dystrophy with regard from the pathologistCHOMETTE, G; AURIOL, M.Revue de stomatologie et de chirurgie maxillo-faciale. 1987, Vol 88, Num 1, pp 15-19, issn 0035-1768Article

Boomerang dysplasiaKOZLOWSKI, K; SILLENCE, D; CORTIS-JONES, R et al.British journal of radiology. 1985, Vol 58, Num 688, pp 369-371, issn 0007-1285Article

Fibrochondrogenesis: radiologic and histologic studiesETESON, D. J; ADOMIAN, G. E; ORNOY, A et al.American journal of medical genetics. 1984, Vol 19, Num 2, pp 277-290, issn 0148-7299Article

A case of skeletal dysplasia with advanced carpal ossification and monkey wrench appearance of the femora : mild Desbuqhois dyplasia ?NISHIMURA, G; SATO, S; OGATA, T et al.European journal of pediatrics. 1996, Vol 155, Num 12, pp 1040-1042, issn 0340-6199Article

Generalized enchondromatosis: a case reportPATERSON, D. C; MORRIS, L. L; BINNS, G. F et al.Journal of bone and joint surgery. American volume. 1989, Vol 71, Num 1, pp 133-140, issn 0021-9355Article

Acro-mesomelic dysplasia ― a new type: report of two siblingsBRAHIMI, L; BACHA, L; KOZLOWSKI, K et al.Pediatric radiology. 1988, Vol 18, Num 1, pp 67-69, issn 0301-0449Article

Osteopetrosis: some unusual radiological features with a short reviewKOLAWOLE, T. M; HAWASS, N. D; PATEL, P. J et al.European journal of radiology. 1988, Vol 8, Num 2, pp 89-95, issn 0720-048XArticle

Ossifizierender Weichteiltumor bei Melorheostose = Ostification des tumeurs des parties molles dans la mélorhéostose = Ostifying saft tissue tumours in melorheostosisHALLER, V. J; WITTICH, G. R; SOMMER, G et al.RöFo. Fortschritte auf dem Gebiete der Röntgenstrahlen und der Nuklearmedizin. 1987, Vol 146, Num 3, pp 358-360, issn 0340-1618Article

Brief clinical report: Sedaghatian congenital lethal metaphyseal chondrodysplasia ― observations in a second Iranian family and histopathological studiesOPITZ, J. M; SPRANGER, J. W; STOSS, H. R et al.American journal of medical genetics. 1987, Vol 26, Num 3, pp 583-590, issn 0148-7299Article

Cytochrome a₃ deficiency in human achondroplasiaMACKLER, B; DAVIS, K. A; GRACE, R et al.Biochimica et biophysica acta. 1987, Vol 891, Num 2, pp 145-149, issn 0006-3002Article

De la Chapelle dysplasiaWHITLEY, C. B; BURKE, B. A; GRANROTH, G et al.American journal of medical genetics. 1986, Vol 25, Num 1, pp 29-39, issn 0148-7299Article

Osteogenesis imperfecta: phenotypic heterogeneity, protein suicide, short and long collagenPROCKOP, D. J.American journal of human genetics. 1984, Vol 36, Num 3, pp 499-505, issn 0002-9297Article

Possible heterogeneity in spondyloenchondrodysplasia : Quadriparesis, basal ganglia calcifications, and chondrocyte inclusionsFRYDMAN, M; BAR-ZIV, J; PREMINGER-SHAPIRO, R et al.American journal of medical genetics. 1990, Vol 36, Num 3, pp 279-284, issn 0148-7299, 6 p.Article

Prevalence of lethal osteochondrodysplasiasCOBBEN, J. M; CORNEL, M. C; DIJKSTRA, I et al.American journal of medical genetics. 1990, Vol 36, Num 3, pp 377-378, issn 0148-7299, 2 p.Article

Case report 486BROWN, D. D; CHILDRESS, M. H.Skeletal radiology. 1988, Vol 17, Num 4, pp 302-305, issn 0364-2348Article

Facial paralysis at the age of 2 months as a first clinical sign of van Buchem disease (endosteal hyperostosis)FRYNS, J. P; VAN DEN BERGHE, H.European journal of pediatrics. 1988, Vol 147, Num 1, pp 99-100, issn 0340-6199Article