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	201.	Radiological and clinical analysis of Madelung's deformity in children. [electronic resource] by Huguet, S Leheup, B Aslan, M Muller, F Dautel, G Journeau, P Producer: 20150720 In: Orthopaedics & traumatology, surgery & research : OTSR vol. 100 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	202.	Improved molecular diagnostics of idiopathic short stature and allied disorders: quantitative polymerase chain reaction-based copy number profiling of SHOX and pseudoautosomal region 1. [electronic resource] by D'haene, Barbara Hellemans, Jan Craen, Margarita De Schepper, Jean Devriendt, Koen Fryns, Jean-Pierre Keymolen, Kathelijn Debals, Eveline de Klein, Annelies de Jong, Elisabeth M Segers, Karin De Paepe, Anne Mortier, Geert Vandesompele, Jo De Baere, Elfride Producer: 20100701 In: The Journal of clinical endocrinology and metabolism vol. 95 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	203.	Analysis of common SHOX gene sequence variants and ~4.9-kb PAR1 deletion in ISS patients. [electronic resource] by Solc, Roman Hirschfeldova, Katerina Kebrdlova, Vera Baxova, Alice Producer: 20150408 In: Journal of genetics vol. 93 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	204.	DNA Methylation Status of SHOX-Flanking CpG Islands in Healthy Individuals and Short Stature Patients with Pseudoautosomal Copy Number Variations. [electronic resource] by Ogushi, Kenichiro Hattori, Atsushi Suzuki, Erina Shima, Hirohito Izawa, Masako Yagasaki, Hideaki Horikawa, Reiko Uetake, Kimiaki Umezawa, Akihiro Ishii, Tomohiro Muroya, Koji Namba, Noriyuki Tanaka, Toshiaki Hirano, Yasuhiro Yamamoto, Hitoshi Soneda, Shun Matsubara, Keiko Kagami, Masayo Miyado, Mami Fukami, Maki Producer: 20190918 In: Cytogenetic and genome research vol. 158 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	205.	Growth hormone is effective in treatment of short stature associated with short stature homeobox-containing gene deficiency: Two-year results of a randomized, controlled, multicenter trial. [electronic resource] by Blum, Werner F Crowe, Brenda J Quigley, Charmian A Jung, Heike Cao, Dachuang Ross, Judith L Braun, LeeAnn Rappold, Gudrun Producer: 20070220 In: The Journal of clinical endocrinology and metabolism vol. 92 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	206.	Hypospadias in a male infant with an unusual mosaic 45,X/46,X,psu idic(Y)(p11.32)/46,XY and haploinsufficiency of SHOX: A case report. [electronic resource] by Si, Yan-Mei Dong, Yuan Wang, Wei Qi, Ke-Yan Wang, Xin Producer: 20180326 In: Molecular medicine reports vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	207.	The short stature homeobox gene SHOX is involved in skeletal abnormalities in Turner syndrome. [electronic resource] by Clement-Jones, M Schiller, S Rao, E Blaschke, R J Zuniga, A Zeller, R Robson, S C Binder, G Glass, I Strachan, T Lindsay, S Rappold, G A Producer: 20000601 In: Human molecular genetics vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	208.	Evaluation of SHOX copy number variations in patients with Müllerian aplasia. [electronic resource] by Sandbacka, Maria Halttunen, Mervi Jokimaa, Varpu Aittomäki, Kristiina Laivuori, Hannele Producer: 20111121 In: Orphanet journal of rare diseases vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	209.	Diagnostic screening identifies a wide range of mutations involving the SHOX gene, including a common 47.5 kb deletion 160 kb downstream with a variable phenotypic effect. [electronic resource] by Bunyan, David J Baker, Kevin R Harvey, John F Thomas, N Simon Producer: 20160415 In: American journal of medical genetics. Part A vol. 161A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	210.	[Novel approaches to the background of developmental abnormalities: clinical genetics of transcription factors]. [electronic resource] by Tészás, Alexandra Kárteszi, Judit Kosztolányi, György Producer: 20060706 In: Orvosi hetilap vol. 147 Availability: No items available. Save to lists Add to cart (remove)
	211.	Pseudoautosomal linkage of Hodgkin disease. [electronic resource] by Whittemore, A S Shih, M C Producer: 20000821 In: American journal of human genetics vol. 67 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	212.	Impairment of SHOX nuclear localization as a cause for Léri-Weill syndrome. [electronic resource] by Sabherwal, Nitin Schneider, Katja U Blaschke, Rüdiger J Marchini, Antonio Rappold, Gudrun Producer: 20051207 In: Journal of cell science vol. 117 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	213.	Quantitative real-time polymerase chain reaction (RQ-PCR) for the rapid detection of SHOX haploinsufficiency in Leri-Weill Syndrome. [electronic resource] by Tan, Yuen-Ming Loke, Kah-Yin Producer: 20060203 In: Diagnostic molecular pathology : the American journal of surgical pathology, part B vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	214.	Transactivation function of an approximately 800-bp evolutionarily conserved sequence at the SHOX 3' region: implication for the downstream enhancer. [electronic resource] by Fukami, Maki Kato, Fumiko Tajima, Toshihiro Yokoya, Susumu Ogata, Tsutomu Producer: 20060530 In: American journal of human genetics vol. 78 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	215.	Impaired GH secretion in patients with SHOX deficiency and efficacy of recombinant human GH therapy. [electronic resource] by Iughetti, Lorenzo Vannelli, Silvia Street, Maria Elisabeth Pirazzoli, Piero Bertelloni, Silvano Radetti, Giorgio Capone, Lucia Stasiowska, Barbara Mazzanti, Laura Gastaldi, Roberto Maggio, Maria Cristina Predieri, Barbara Producer: 20130722 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)
	216.	Height gains in response to growth hormone treatment to final height are similar in patients with SHOX deficiency and Turner syndrome. [electronic resource] by Blum, Werner F Cao, Dachuang Hesse, Volker Fricke-Otto, Susanne Ross, Judith L Jones, Christine Quigley, Charmian A Binder, Gerhard Producer: 20090507 In: Hormone research vol. 71 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	217.	Clinical and radiological characteristics of 22 children with SHOX anomalies and familial short stature suggestive of Léri-Weill Dyschondrosteosis. [electronic resource] by Salmon-Musial, Anne-Sophie Rosilio, Myriam David, Michel Huber, Céline Pichot, Emmanuel Cormier-Daire, Valérie Nicolino, Marc Producer: 20120201 In: Hormone research in paediatrics vol. 76 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	218.	Turner syndrome and Xp deletions: clinical and molecular studies in 47 patients. [electronic resource] by Ogata, T Muroya, K Matsuo, N Shinohara, O Yorifuji, T Nishi, Y Hasegawa, Y Horikawa, R Tachibana, K Producer: 20011213 In: The Journal of clinical endocrinology and metabolism vol. 86 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	219.	Deletion of the pseudoautosomal region in a male with a unique Y;13 translocation and short stature. [electronic resource] by Shanske, A Ellison, J Vuguin, P Dowling, P Wasserman, E Heinrich, J Saenger, P Producer: 19990330 In: American journal of medical genetics vol. 82 Availability: No items available. Save to lists Add to cart (remove)
	220.	Height matters-from monogenic disorders to normal variation. [electronic resource] by Durand, Claudia Rappold, Gudrun A Producer: 20130805 In: Nature reviews. Endocrinology vol. 9 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 296 results.