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	101.	Acute lymphoblastic leukemia in a child with Leri-Weill syndrome and complete SHOX gene deletion: A Case Report. [electronic resource] by Volejnikova, Jana Zapletalova, Jirina Jarosova, Marie Urbankova, Helena Petr, Vojta Klaskova, Eva Horwitz, Marshall S Hajduch, Marian Mihal, Vladimir Producer: 20180926 In: Biomedical papers of the Medical Faculty of the University Palacky, Olomouc, Czechoslovakia vol. 162 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	102.	Short stature in a mother and daughter caused by familial der(X)t(X;X)(p22.1-3;q26). [electronic resource] by Reinehr, T Jauch, A Zoll, B Engel, U Bartels, I Andler, W Producer: 20010823 In: American journal of medical genetics vol. 102 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	103.	A duplication encompassing the SHOX gene and the downstream evolutionarily conserved sequences. [electronic resource] by Roos, Laura Brøndum Nielsen, Karen Tümer, Zeynep Producer: 20100127 In: American journal of medical genetics. Part A vol. 149A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	104.	A rare case of a male with 45, XO, SRY+, ZFY+ with short stature and mild Turner stigmata. [electronic resource] by Ntali, Georgia Sofocleous, Christalena Kouvidi, Elisabeth Tsagaraki, Georgia Dolianiti, Maria Kaimara-Papathanasiou, Asteroula Fryssira, Helen Producer: 20130201 In: Hormone research in paediatrics vol. 78 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	105.	A short history of the initial discovery of the SHOX gene. [electronic resource] by Bernasconi, S Garavelli, L Producer: 20130409 In: Journal of endocrinological investigation vol. 33 Availability: No items available. Save to lists Add to cart (remove)
	106.	Different approaches in the molecular analysis of the SHOX gene dysfunctions. [electronic resource] by Stuppia, L Gatta, V Antonucci, I Giuliani, R Palka, G Producer: 20130409 In: Journal of endocrinological investigation vol. 33 Availability: No items available. Save to lists Add to cart (remove)
	107.	A Deletion of More than 800 kb Is the Most Recurrent Mutation in Chilean Patients with SHOX Gene Defects. [electronic resource] by Poggi, Helena Vera, Alejandra Avalos, Carolina Lagos, Marcela Mellado, Cecilia Aracena, Mariana Aravena, Teresa Garcia, Hernan Godoy, Claudia Cattani, Andreina Reyes, Loreto Lacourt, Patricia Rumie, Hana Mericq, Veronica Arriaza, Marta Martinez-Aguayo, Alejandro Producer: 20160912 In: Hormone research in paediatrics vol. 84 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	108.	Co-occurrence of genomic imbalances on Xp22.1 in the SHOX region and 15q25.2 in a girl with short stature, precocious puberty, urogenital malformations and bone anomalies. [electronic resource] by Monzani, Alice Babu, Deepak Mellone, Simona Genoni, Giulia Fanelli, Antonella Prodam, Flavia Bellone, Simonetta Giordano, Mara Producer: 20200106 In: BMC medical genomics vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	109.	SHOX point mutations in dyschondrosteosis. [electronic resource] by Huber, C Cusin, V Le Merrer, M Mathieu, M Sulmont, V Dagoneau, N Munnich, A Cormier-Daire, V Producer: 20011018 In: Journal of medical genetics vol. 38 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	110.	Pseudodominant inheritance of Langer mesomelic dysplasia caused by a SHOX homeobox missense mutation. [electronic resource] by Shears, Deborah J Guillen-Navarro, Encarna Sempere-Miralles, Manuel Domingo-Jimenez, Rosario Scambler, Peter J Winter, Robin M Producer: 20020920 In: American journal of medical genetics vol. 110 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	111.	The SHOX gene: a new indication for GH treatment. [electronic resource] by Cicognani, A Pirazzoli, P Nicoletti, A Baronio, F Conti, V Bonetti, S Producer: 20130409 In: Journal of endocrinological investigation vol. 33 Availability: No items available. Save to lists Add to cart (remove)
	112.	Height outcome of the recombinant human growth hormone treatment in patients with SHOX gene haploinsufficiency: a meta-analysis. [electronic resource] by Massart, Francesco Bizzi, Martina Baggiani, Angelo Miccoli, Mario Producer: 20140207 In: Pharmacogenomics vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	113.	Increased cortical area and thickness in the distal radius in subjects with SHOX-gene mutation. [electronic resource] by Frederiksen, A L Hansen, S Brixen, K Frost, M Producer: 20150731 In: Bone vol. 69 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	114.	A Rare Variant of Turner Syndrome in Four Sequential Generations: Effect of the Interplay of Growth Hormone Treatment and Estrogens on Body Proportion. [electronic resource] by Stoklasova, Judith Kaprova, Jana Trkova, Marie Nedomova, Vera Zemkova, Dana Matyskova, Jana Soucek, Ondrej Sumnik, Zdenek Lebl, Jan Producer: 20170417 In: Hormone research in paediatrics vol. 86 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	115.	Longitudinal auxological study in a female with SHOX (short stature homeobox containing gene) haploinsufficiency and normal ovarian function. [electronic resource] by Fukami, Maki Matsuo, Nobutake Hasegawa, Tomonobu Sato, Seiji Ogata, Tsutomu Producer: 20031118 In: European journal of endocrinology vol. 149 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	116.	SHOX gene defects and selected dysmorphic signs in patients of idiopathic short stature and Léri-Weill dyschondrosteosis. [electronic resource] by Hirschfeldova, K Solc, R Baxova, A Zapletalova, J Kebrdlova, V Gaillyova, R Prasilova, S Soukalova, J Mihalova, R Lnenicka, P Florianova, M Stekrova, J Producer: 20120118 In: Gene vol. 491 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	117.	Identification of a novel SHOX mutation in a Chinese family with isolated Madelung deformity. [electronic resource] by Mei, Libin Huang, Yanru Pan, Qian Li, Haoxian Liang, Desheng Wu, Lingqian Producer: 20150828 In: Journal of genetics vol. 93 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	118.	Genotype and phenotype in paediatric endocrine practice. [electronic resource] by Donaghue, K C Producer: 20010315 In: Trends in endocrinology and metabolism: TEM vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	119.	Langer mesomelic dysplasia in early fetuses: two cases and a literature review. [electronic resource] by Ambrosetti, Fabrizio Palicelli, Andrea Bulfamante, Gaetano Rivasi, Francesco Producer: 20141020 In: Fetal and pediatric pathology vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	120.	Anthropometric evaluation of children with SHOX mutations can be used as indication for genetic studies in children of short stature. [electronic resource] by Jorge, Alexander A L Arnhold, Ivo J P Producer: 20071023 In: Journal of medical genetics vol. 44 Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 296 results.