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	281.	The role of the SHOX gene in the pathophysiology of Turner syndrome. [electronic resource] by Oliveira, Conceicao S Alves, Cresio Producer: 20120203 In: Endocrinologia y nutricion : organo de la Sociedad Espanola de Endocrinologia y Nutricion vol. 58 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	282.	SHOX duplications found in some cases with type I Mayer-Rokitansky-Kuster-Hauser syndrome. [electronic resource] by Gervasini, Cristina Grati, Francesca Romana Lalatta, Faustina Tabano, Silvia Gentilin, Barbara Colapietro, Patrizia De Toffol, Simona Frontino, Giada Motta, Francesca Maitz, Silvia Bernardini, Laura Dallapiccola, Bruno Fedele, Luigi Larizza, Lidia Miozzo, Monica Producer: 20110131 In: Genetics in medicine : official journal of the American College of Medical Genetics vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	283.	SHOX mutations in a family and a fetus with Langer mesomelic dwarfism. [electronic resource] by Thomas, N Simon Maloney, Viv Bass, Paul Mulik, Varsha Wellesley, Diana Castle, Bruce Producer: 20050112 In: American journal of medical genetics. Part A vol. 128A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	284.	Clinical utility gene card for: Mayer-Rokitansky-Küster-Hauser syndrome. [electronic resource] by Morcel, Karine Dallapiccola, Bruno Pasquier, Laurent Watrin, Tanguy Bernardini, Laura Guerrier, Daniel Producer: 20120507 In: European journal of human genetics : EJHG vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	285.	Structural and numerical changes of chromosome X in patients with esophageal atresia. [electronic resource] by Brosens, Erwin de Jong, Elisabeth M Barakat, Tahsin Stefan Eussen, Bert H D'haene, Barbara De Baere, Elfride Verdin, Hannah Poddighe, Pino J Galjaard, Robert-Jan Gribnau, Joost Brooks, Alice S Tibboel, Dick de Klein, Annelies Producer: 20150413 In: European journal of human genetics : EJHG vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	286.	Retinoic acid catabolizing enzyme CYP26C1 is a genetic modifier in SHOX deficiency. [electronic resource] by Montalbano, Antonino Juergensen, Lonny Roeth, Ralph Weiss, Birgit Fukami, Maki Fricke-Otto, Susanne Binder, Gerhard Ogata, Tsutomu Decker, Eva Nuernberg, Gudrun Hassel, David Rappold, Gudrun A Producer: 20170922 In: EMBO molecular medicine vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	287.	FGFR3 is a target of the homeobox transcription factor SHOX in limb development. [electronic resource] by Decker, Eva Durand, Claudia Bender, Sebastian Rödelsperger, Christian Glaser, Anne Hecht, Jochen Schneider, Katja U Rappold, Gudrun Producer: 20110721 In: Human molecular genetics vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	288.	Detection of Turner Syndrome by quantitative PCR of SHOX and VAMP7 genes. [electronic resource] by Ibarra-Ramírez, Marisol Zamudio-Osuna, Michelle Jesús Campos-Acevedo, Luis Daniel Gallardo-Blanco, Hugo Leonid Cerda-Flores, Ricardo Martin Rodríguez-Sánchez, Irám Pablo Martínez-de-Villarreal, Laura Elia Producer: 20151022 In: Genetic testing and molecular biomarkers vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	289.	Phenotypic variation and genetic heterogeneity in Léri-Weill syndrome. [electronic resource] by Schiller, S Spranger, S Schechinger, B Fukami, M Merker, S Drop, S L Tröger, J Knoblauch, H Kunze, J Seidel, J Rappold, G A Producer: 20000414 In: European journal of human genetics : EJHG vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	290.	A novel point mutation A170P in the SHOX gene defines impaired nuclear translocation as a molecular cause for Léri-Weill dyschondrosteosis and Langer dysplasia. [electronic resource] by Sabherwal, N Blaschke, R J Marchini, A Heine-Suner, D Rosell, J Ferragut, J Blum, W F Rappold, G Producer: 20040927 In: Journal of medical genetics vol. 41 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	291.	The homeobox transcription factor HOXA9 is a regulator of SHOX in U2OS cells and chicken micromass cultures. [electronic resource] by Durand, Claudia Decker, Eva Roeth, Ralph Schneider, Katja U Rappold, Gudrun Producer: 20130225 In: PloS one vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	292.	SHOX interacts with the chondrogenic transcription factors SOX5 and SOX6 to activate the aggrecan enhancer. [electronic resource] by Aza-Carmona, Miriam Shears, Debbie J Yuste-Checa, Patricia Barca-Tierno, Verónica Hisado-Oliva, Alfonso Belinchón, Alberta Benito-Sanz, Sara Rodríguez, J Ignacio Argente, Jesús Campos-Barros, Angel Scambler, Peter J Heath, Karen E Producer: 20110721 In: Human molecular genetics vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	293.	Transcriptional and translational regulation of the Leri-Weill and Turner syndrome homeobox gene SHOX. [electronic resource] by Blaschke, Rudiger J Töpfer, Christine Marchini, Antonio Steinbeisser, Herbert Janssen, Johannes W G Rappold, Gudrun A Producer: 20040112 In: The Journal of biological chemistry vol. 278 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	294.	SHOT, a SHOX-related homeobox gene, is implicated in craniofacial, brain, heart, and limb development. [electronic resource] by Blaschke, R J Monaghan, A P Schiller, S Schechinger, B Rao, E Padilla-Nash, H Ried, T Rappold, G A Producer: 19980409 In: Proceedings of the National Academy of Sciences of the United States of America vol. 95 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	295.	Long-range conserved non-coding SHOX sequences regulate expression in developing chicken limb and are associated with short stature phenotypes in human patients. [electronic resource] by Sabherwal, Nitin Bangs, Fiona Röth, Ralph Weiss, Birgit Jantz, Karin Tiecke, Eva Hinkel, Georg K Spaich, Christiane Hauffa, Berthold P van der Kamp, Hetty Kapeller, Johannes Tickle, Cheryll Rappold, Gudrun Producer: 20070405 In: Human molecular genetics vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	296.	The short stature homeodomain protein SHOX induces cellular growth arrest and apoptosis and is expressed in human growth plate chondrocytes. [electronic resource] by Marchini, Antonio Marttila, Tiina Winter, Anja Caldeira, Sandra Malanchi, Ilaria Blaschke, Rüdiger J Häcker, Beate Rao, Ercole Karperien, Marcel Wit, Jan M Richter, Wiltrud Tommasino, Massimo Rappold, Gudrun A Producer: 20041006 In: The Journal of biological chemistry vol. 279 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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