These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
5. Transcription factor SOX3 is involved in X-linked mental retardation with growth hormone deficiency. Laumonnier F, Ronce N, Hamel BC, Thomas P, Lespinasse J, Raynaud M, Paringaux C, Van Bokhoven H, Kalscheuer V, Fryns JP, Chelly J, Moraine C, Briault S. Am J Hum Genet; 2002 Dec; 71(6):1450-5. PubMed ID: 12428212 [Abstract] [Full Text] [Related]
6. X-linked congenital hypertrichosis syndrome is associated with interchromosomal insertions mediated by a human-specific palindrome near SOX3. Zhu H, Shang D, Sun M, Choi S, Liu Q, Hao J, Figuera LE, Zhang F, Choy KW, Ao Y, Liu Y, Zhang XL, Yue F, Wang MR, Jin L, Patel PI, Jing T, Zhang X. Am J Hum Genet; 2011 Jun 10; 88(6):819-826. PubMed ID: 21636067 [Abstract] [Full Text] [Related]
8. Studies of mice deleted for Sox3 and uc482: relevance to X-linked hypoparathyroidism. Gaynor KU, Grigorieva IV, Mirczuk SM, Piret S, Kooblall KG, Stevenson M, Rizzoti K, Bowl MR, Nesbit MA, Christie PT, Fraser WD, Hough T, Whyte MP, Lovell-Badge R, Thakker R. Endocr Connect; 2020 Jan 01; 9(2):173-86. PubMed ID: 31961795 [Abstract] [Full Text] [Related]
9. [Idiopathic hypoparathyroidism due to abnormalities in parathyroid organogenesis]. Tanaka H. Clin Calcium; 2007 Aug 01; 17(8):1206-13. PubMed ID: 17660617 [Abstract] [Full Text] [Related]
12. Over- and underdosage of SOX3 is associated with infundibular hypoplasia and hypopituitarism. Woods KS, Cundall M, Turton J, Rizotti K, Mehta A, Palmer R, Wong J, Chong WK, Al-Zyoud M, El-Ali M, Otonkoski T, Martinez-Barbera JP, Thomas PQ, Robinson IC, Lovell-Badge R, Woodward KJ, Dattani MT. Am J Hum Genet; 2005 May 01; 76(5):833-49. PubMed ID: 15800844 [Abstract] [Full Text] [Related]
13. Duplication of Xq26.2-q27.1, including SOX3, in a mother and daughter with short stature and dyslalia. Stankiewicz P, Thiele H, Schlicker M, Cseke-Friedrich A, Bartel-Friedrich S, Yatsenko SA, Lupski JR, Hansmann I. Am J Med Genet A; 2005 Sep 15; 138(1):11-7. PubMed ID: 16097007 [Abstract] [Full Text] [Related]
14. A family with X-linked anophthalmia: exclusion of SOX3 as a candidate gene. Slavotinek A, Lee SS, Hamilton SP. Am J Med Genet A; 2005 Oct 01; 138A(2):89-94. PubMed ID: 16114045 [Abstract] [Full Text] [Related]
18. Polyalanine expansion mutations in the X-linked hypopituitarism gene SOX3 result in aggresome formation and impaired transactivation. Wong J, Farlie P, Holbert S, Lockhart P, Thomas PQ. Front Biosci; 2007 Jan 01; 12():2085-95. PubMed ID: 17127446 [Abstract] [Full Text] [Related]
19. SOX3 is an X-linked gene related to SRY. Stevanović M, Lovell-Badge R, Collignon J, Goodfellow PN. Hum Mol Genet; 1993 Dec 01; 2(12):2013-8. PubMed ID: 8111369 [Abstract] [Full Text] [Related]