Your search returned 63 results.

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	21.	Opalescent dentine in two affected siblings. [electronic resource] by Mahoney, E K Widmer, R P Sillence, D O Producer: 20010712 In: The New Zealand dental journal vol. 97 Availability: No items available. Save to lists Add to cart (remove)
	22.	Fibrochondrogenesis in male twins at 24 weeks gestation. [electronic resource] by Bankier, A Fortune, D Duke, J Sillence, D O Producer: 19910509 In: American journal of medical genetics vol. 38 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	23.	Comparisons and correlations of skeletal defects in mouse and human. [electronic resource] by Rimoin, D L Eteson, D J Sillence, D O Producer: 19890316 In: Pathology and immunopathology research vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	24.	Animal model: skeletal anomalies in mice with cleidocranial dysplasia. [electronic resource] by Sillence, D O Ritchie, H E Selby, P B Producer: 19870724 In: American journal of medical genetics vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	25.	Clinical variability in osteogenesis imperfecta-variable expressivity or genetic heterogeneity. [electronic resource] by Sillence, D O Rimoin, D L Danks, D M Producer: 19800417 In: Birth defects original article series vol. 15 Availability: No items available. Save to lists Add to cart (remove)
	26.	Abnormalities of the spine in Goldenhar's syndrome. [electronic resource] by Gibson, J N Sillence, D O Taylor, T K Producer: 19961105 In: Journal of pediatric orthopedics vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	27.	Desbuquois syndrome: clinical and radiological report of the first two Chinese cases from a consanguineous family. [electronic resource] by Lam, W F Chan, H B Sillence, D O Producer: 20080327 In: Journal of paediatrics and child health vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	28.	Congenital synspondylism. [electronic resource] by Wiles, C R Taylor, T F Sillence, D O Producer: 19920323 In: American journal of medical genetics vol. 42 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	29.	Axenfeld anomaly in association with hypomelanosis of Ito. [electronic resource] by Flaherty, M P Padilla, C D Sillence, D O Producer: 19911001 In: Ophthalmic paediatrics and genetics vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	30.	Achondroplasia and zinc deficiency. [electronic resource] by Wassman, E R Rimoin, D L Sillence, D O Greenberg, D Producer: 19801125 In: The Journal of pediatrics vol. 97 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	31.	Spondylometaphyseal dysplasia Sedaghatian type associated with lethal arrhythmia and normal intrauterine growth in three siblings. [electronic resource] by Kerr, B Smith, V Patel, R Ladusans, E Sillence, D O Producer: 20001207 In: Clinical dysmorphology vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	32.	Desbuquois syndrome complicated by obstructive sleep apnoea and cervical kyphosis. [electronic resource] by Ogle, R F Wilson, M J Kozlowski, K Sillence, D O Producer: 19940923 In: American journal of medical genetics vol. 51 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	33.	Ehlers-Danlos syndrome type IV: phenotypic consequences of a splicing mutation in one COL3A1 allele. [electronic resource] by Sillence, D O Chiodo, A A Campbell, P E Cole, W G Producer: 19920204 In: Journal of medical genetics vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	34.	Fragilitas ossium (fro/fro) in the mouse: a model for a recessively inherited type of osteogenesis imperfecta. [electronic resource] by Sillence, D O Ritchie, H E Dibbayawan, T Eteson, D Brown, K Producer: 19930422 In: American journal of medical genetics vol. 45 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	35.	Abnormal type III collagen produced by an exon-17-skipping mutation of the COL3A1 gene in Ehlers-Danlos syndrome type IV is not incorporated into the extracellular matrix. [electronic resource] by Chiodo, A A Sillence, D O Cole, W G Bateman, J F Producer: 19951221 In: The Biochemical journal vol. 311 ( Pt 3) Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	36.	The mouse skeletal mutants: models for the human skeletal dysplasias. [electronic resource] by Eteson, D J Sillence, D O Lachman, R S Rimoin, D L Producer: 19851127 In: Progress in clinical and biological research vol. 187 Availability: No items available. Save to lists Add to cart (remove)
	37.	A common presentation of a rare genetic disorder clinically mimicking primary myopathy. [electronic resource] by Wu, K H C Kohn, M R Turner, A Sillence, D O Producer: 20121204 In: Adolescent medicine: state of the art reviews vol. 23 Availability: No items available. Save to lists Add to cart (remove)
	38.	Optometric screening in achondroplasia, diastrophic dysplasia, and spondyloepiphyseal dysplasia congenita. [electronic resource] by Griffin, J R Ault, J E Sillence, D O Rimoin, D L Producer: 19800712 In: American journal of optometry and physiological optics vol. 57 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	39.	The phenotypic features of osteogenesis imperfecta resulting from a mutation of the carboxyl-terminal pro alpha 1 (I) propeptide that impairs the assembly of type I procollagen and formation of the extracellular matrix. [electronic resource] by Cole, W G Chow, C W Bateman, J F Sillence, D O Producer: 19970313 In: Journal of medical genetics vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	40.	Spondylohumerofemoral hypoplasia (giant cell chondrodysplasia): a neonatally lethal short-limbed skeletal displasia. [electronic resource] by Sillence, D O Lachman, R S Jenkins, T Riccardi, V M Rimoin, D L Producer: 19821216 In: American journal of medical genetics vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 63 results.