The human genome projectSILLENCE, D.Medical journal of Australia. 1990, Vol 152, Num 9, pp 486-488, issn 0025-729XArticle

MALFORMATION SYNDROME OF CHROMOSOME 109 DUPLICATION AND THE VATER ASSOCIATIONFIELD B; SMITH A; SILLENCE D et al.1983; ANNALES DE GENETIQUE; ISSN 0003-3995; FRA; DA. 1983; VOL. 26; NO 1; PP. 31-33; ABS. FRE; BIBL. 18 REF.Article

AN EMBEDDING METHOD FOR HISTOCHEMICAL STUDIES OF UNDECALCIFIED SKELETAL GROWTH PLATEHORTON WA; DOCKERY N; SILLENCE D et al.1980; STAIN TECHNOL.; USA; DA. 1980; VOL. 55; NO 1; PP. 19-29; BIBL. 2 P.Article

A METHOD FOR UNIFORM POLYMERIZATION OF LARGE BLOCKS OF CHONDRO-OSSEOUS TISSUE EMBEDDED IN GLYCOL METHACRYLATEHAMILTON R; SILLENCE D; SHIMONO L et al.1979; STAIN TECHNOL.; USA; DA. 1979; VOL. 54; NO 4; PP. 220-221; BIBL. 4 REF.Article

Familial Scheuermann disease : a genetic and linkage studyMCKENZIE, L; SILLENCE, D.Journal of medical genetics. 1992, Vol 29, Num 1, pp 41-45, issn 0022-2593Article

Variability in kyphomelic dysplasiaCISARIK, F; KOZLOWSKI, K; MASEL, J et al.Pediatric radiology. 1999, Vol 29, Num 7, pp 551-557, issn 0301-0449Article

Subcellular distribution of agonist-stimulated phosphatidylinositol synthesis in 1321 N1 astrocytoma cellsSILLENCE, D. J; DOWNES, C. P.Biochemical journal (London. 1984). 1993, Vol 290, pp 381-387, issn 0264-6021, 2Article

Lithium treatment of affective disorders : effects of lithium on the inositol phospholipid and cyclic AMP signalling pathwaysSILLENCE, D. J; DOWNES, C. P.Biochimica et biophysica acta. Molecular basis of disease. 1992, Vol 1138, Num 1, pp 46-52Article

The clinical features of Ehlers-Danlos syndrome type VII due to a deletion of 24 amino acids from the pro_α(I) chain of type ICOLE, W. G; EVANS, R; SILLENCE, D. O et al.Journal of medical genetics. 1987, Vol 24, Num 11, pp 698-701, issn 0022-2593Article

Case report 870SILLENCE, D; DELPRADO, W; EDWARDS, M et al.Skeletal radiology. 1994, Vol 23, Num 7, pp 586-588, issn 0364-2348Article

DIASTROPHIC DYSPLASIA: THE DEATH OF A VARIANTLACHMAN R; SILLENCE D; RIMOIN D et al.1981; RADIOLOGY; ISSN 0033-8419; USA; DA. 1981; VOL. 140; NO 1; PP. 79-86; BIBL. 14 REF.Article

ADRENOLEUKODYSTROPHY: EVIDENCE FOR X LINKAGE, INACTIVATION, AND SELECTION FAVORING THE MUTANT ALLELE IN HETEROZYGOUS CELLSMIGEON BR; MOSER HW; MOSER AB et al.1981; PROC. NATL. ACAD. SCI. U.S.A., BIOL. SCI.; ISSN 0273-1134; USA; DA. 1981; VOL. 78; NO 8; PP. 5066-5070; BIBL. 18 REF.Article

Craniocervical abnormalities in osteogenesis imperfecta: genetic and molecular correlationSILLENCE, D. O.Pediatric radiology. 1994, Vol 24, Num 6, pp 427-430, issn 0301-0449Conference Paper

Lumbar platsypondyly : characteristic sign of Ehlers-Danlos syndromeKOZLOWSKI, K; PADILLA, C; SILLENCE, D et al.Skeletal radiology. 1991, Vol 20, Num 8, pp 589-590, issn 0364-2348Article

The rib gap anomaly in partial or mosaic trisomy 8KOZLOWSKI, K; COLLIS, J; SUTER, M et al.Skeletal radiology. 1988, Vol 17, Num 4, pp 251-254, issn 0364-2348Article

Short stature, mental retardation, craniosynostosis, Klippel-Feil syndrome, Scheuerman kyphosis, rib gaps and other distinctive skeletal and genital anomalies. A new syndrome?KOZLOWSKI, K; SILLENCE, D; TAYLOR, F et al.Pediatric radiology. 1993, Vol 23, Num 6, pp 442-445, issn 0301-0449Article

An X-linked reticulate pigmentary disorder with systemic manifestations: report of a second familyADES, L. C; ROGERS, M; SILLENCE, D. O et al.Pediatric dermatology. 1993, Vol 10, Num 4, pp 344-351, issn 0736-8046Article

Natural history of blue sclerae in osteogenesis imperfectaSILLENCE, D; BUTLER, B; LATHAM, M et al.American journal of medical genetics. 1993, Vol 45, Num 2, pp 183-186, issn 0148-7299Conference Paper

A new syndrome? Unusual facies, hooked clavicles, 13 pairs of ribs, widened metaphyses, square shaped vertebral bodies and communicating hydrocephalusKOZLOWSKI, K; BROWN, J; HARDWICK, R et al.Pediatric radiology. 1992, Vol 22, Num 5, pp 328-330, issn 0301-0449Article

Lethal micromelic facial bones sclerosis dysplasiaMÜLLER, D; KOZLOWSKI, K; SILLENCE, D et al.British journal of radiology. 1992, Vol 65, Num 780, pp 1137-1139, issn 0007-1285Article

Dappled diaphyseal dysplasiasCARTY, H; KOZLOWSKI, K; SILLENCE, D et al.RöFo. Fortschritte auf dem Gebiete der Röntgenstrahlen und der Nuklearmedizin. 1989, Vol 150, Num 2, pp 228-229, issn 0340-1618Article

Basilar impression complicating osteogenesis imperfecta type IV: the clinical and neuroradiological findings in four casesHAYES, M; PARKER, G; ELL, J et al.Journal of neurology, neurosurgery and psychiatry. 1999, Vol 66, Num 3, pp 357-364, issn 0022-3050Article

Dyssegmental dysplasia (report of two cases with a review of the literature)FASANELLI, S; KOZLOWSKI, K; REITER, S et al.Skeletal radiology. 1985, Vol 14, Num 3, pp 173-177, issn 0364-2348Article

Fragilitas ossium (fro/fro) in the mouse : a model for a recessively inherited type of osteogenesis imperfectaSILLENCE, D. O; SILLENCE, D. O et al.RITCHIE, H. E; SILLENCE, D. O; SILLENCE, D. O et al.RITCHIE, H. E; American journal of medical genetics. 1993, Vol 45, Num 2, pp 276-283, issn 0148-7299Conference Paper

Animal model: skeletal anomalies in mice with cleidocranial dysplasiaSILLENCE, D. O; RITCHIE, H. E; SELBY, P. B et al.American journal of medical genetics. 1987, Vol 27, Num 1, pp 75-85, issn 0148-7299Article