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	21.	Assessing the general population frequency of rare coding variants in the EXT1 and EXT2 genes previously implicated in hereditary multiple exostoses. [electronic resource] by Cousminer, Diana L Arkader, Alexandre Voight, Benjamin F Pacifici, Maurizio Grant, Struan F A Producer: 20180103 In: Bone vol. 92 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	22.	Tiling resolution array-CGH shows that somatic mosaic deletion of the EXT gene is causative in EXT gene mutation negative multiple osteochondromas patients. [electronic resource] by Szuhai, Károly Jennes, Ivy de Jong, Danielle Bovée, Judith V M G Wiweger, Malgorzata Wuyts, Wim Hogendoorn, Pancras C W Producer: 20110324 In: Human mutation vol. 32 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	23.	Novel human pathological mutations. Gene symbol: EXT1. Disease: multiple exostoses. [electronic resource] by Lin, Wei-De Tsai, Fuu-Jer Producer: 20110506 In: Human genetics vol. 127 Availability: No items available. Save to lists Add to cart (remove)
	24.	Heparan sulfate as a regulator of endochondral ossification and osteochondroma development. [electronic resource] by Jochmann, Katja Bachvarova, Velina Vortkamp, Andrea Producer: 20141230 In: Matrix biology : journal of the International Society for Matrix Biology vol. 34 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	25.	Heparan sulfate abnormalities in exostosis growth plates. [electronic resource] by Hecht, J T Hall, C R Snuggs, M Hayes, E Haynes, R Cole, W G Producer: 20030115 In: Bone vol. 31 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	26.	Mutational Analysis of Exostosin 1 and 2 Genes in Multiple Osteochondroma. [electronic resource] by Malini, K Gudi, Narayan S Kutty, A V M Balakrishna, Sharath Producer: 20161215 In: Indian journal of pediatrics vol. 82 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	27.	Differentiation-induced loss of heparan sulfate in human exostosis derived chondrocytes. [electronic resource] by Hecht, Jacqueline T Hayes, Elizabeth Haynes, Richard Cole, William G Long, Robert J Farach-Carson, Mary C Carson, Daniel D Producer: 20051018 In: Differentiation; research in biological diversity vol. 73 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	28.	A novel EXT2 mutation in a consanguineous family with severe developmental delay, microcephaly, seizures, feeding difficulties, and osteopenia extends the phenotypic spectrum of autosomal recessive EXT2-related syndrome (AREXT2). [electronic resource] by El-Bazzal, Lara Atkinson, Alexandre Gillart, Anne-Celine Obeid, Marc Delague, Valérie Mégarbané, André Producer: 20190401 In: European journal of medical genetics vol. 62 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	29.	[Identification of pathogenic variations in two Chinese pedigrees affected with hereditary multiple exostosis]. [electronic resource] by You, Yi Li, Shan Yang, Bo Zhao, Xiuli Producer: 20190924 In: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics vol. 36 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	30.	Genetic screening of EXT1 and EXT2 in Cypriot families with hereditary multiple osteochondromas. [electronic resource] by Tanteles, George A Nicolaou, Michael Neocleous, Vassos Shammas, Christos Loizidou, Maria A Alexandrou, Angelos Ellina, Elena Patsia, Nasia Sismani, Carolina Phylactou, Leonidas A Christophidou-Anastasiadou, Violetta Producer: 20161103 In: Journal of genetics vol. 94 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	31.	Identification of a novel mutation in EXT2 in a fourth-generation Korean family with multiple osteochondromas and overview of mutation spectrum. [electronic resource] by Yang, Aram Kim, Jinsup Jang, Ja-Hyun Lee, Chung Lee, Ji-Eun Cho, Sung Yoon Jin, Dong-Kyu Producer: 20200129 In: Annals of human genetics vol. 83 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	32.	Novel mutations of EXT1 and EXT2 genes among families and sporadic cases with multiple exostoses. [electronic resource] by Pei, Yuanyuan Wang, Yiming Huang, Weijun Hu, Bin Huang, Dongsheng Zhou, Yan Su, Peiqiang Producer: 20110318 In: Genetic testing and molecular biomarkers vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	33.	Axon sorting in the optic tract requires HSPG synthesis by ext2 (dackel) and extl3 (boxer). [electronic resource] by Lee, Jeong-Soo von der Hardt, Sophia Rusch, Melissa A Stringer, Sally E Stickney, Heather L Talbot, William S Geisler, Robert Nüsslein-Volhard, Christiane Selleck, Scott B Chien, Chi-Bin Roehl, Henry Producer: 20050222 In: Neuron vol. 44 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	34.	EXTra hit for mouse osteochondroma. [electronic resource] by Bovée, Judith V M G Producer: 20100305 In: Proceedings of the National Academy of Sciences of the United States of America vol. 107 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	35.	[From gene to disease; hereditary multiple exostoses]. [electronic resource] by Wuyts, W Bovée, J V M G Hogendoorn, P C W Producer: 20020306 In: Nederlands tijdschrift voor geneeskunde vol. 146 Availability: No items available. Save to lists Add to cart (remove)
	36.	A de novo mutation in the EXT2 gene associated with osteochondromatosis in a litter of American Staffordshire Terriers. [electronic resource] by Friedenberg, Steven G Vansteenkiste, Daniella Yost, Oriana Treeful, Amy E Meurs, Kathryn M Tokarz, Debra A Olby, Natasha J Producer: 20181004 In: Journal of veterinary internal medicine vol. 32 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	37.	Identification of Novel EXT Mutations in Patients with Hereditary Multiple Exostoses Using Whole-Exome Sequencing. [electronic resource] by Liang, Chao Wang, Yong-Jie Wei, Yu-Xuan Dong, Yang Zhang, Zhi-Chang Producer: 20201216 In: Orthopaedic surgery vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	38.	Short digits...what's up? [electronic resource] by Aarntzen, E H J G Barrera, P Producer: 20080207 In: Arthritis and rheumatism vol. 57 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	39.	The role of EXT1 gene mutation and its high expression of calcitonin gene-related peptide in the development of multiple exostosis. [electronic resource] by Wu, Zhao-Yang Wang, Yan Wang, Jing-Wen Chen, Yong-Zhong Guo, Yujia Producer: 20190520 In: Biochemical and biophysical research communications vol. 505 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	40.	The heparanome and regulation of cell function: structures, functions and challenges. [electronic resource] by Ori, Alessandro Wilkinson, Mark Charles Fernig, David Garth Producer: 20080919 In: Frontiers in bioscience : a journal and virtual library 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 201 results.