Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Syndrome and FOXP1[original query] |
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Assessing the impact of FOXP1 mutations on developmental verbal dyspraxia. European journal of human genetics : EJHG 2009 Oct 17 (10): 1354-8. Vernes Sonja C, MacDermot Kay D, Monaco Anthony P, Fisher Simon |
Genetic abnormalities in FOXP1 are associated with congenital heart defects. Human mutation 2013 Sep 34 (9): 1226-30. Chang Sheng-Wei, Mislankar Mona, Misra Chaitali, Huang Nianyuan, Dajusta Daniel G, Harrison Steven M, McBride Kim L, Baker Linda A, Garg Vi |
Three Japanese patients with 3p13 microdeletions involving FOXP1. Brain & development 2018 11 41 (3): 257-262. Yamamoto-Shimojima Keiko, Okamoto Nobuhiko, Matsumura Wataru, Okazaki Tetsuya, Yamamoto Toshiyu |
Genetic heterogeneity of disorders with overgrowth and intellectual disability: Experience from a center in North India. American journal of medical genetics. Part A 2021 5 185 (8): 2345-2355. Moirangthem Amita, Mandal Kausik, Saxena Deepti, Srivastava Priyanka, Gambhir Poonam Singh, Agrawal Neha, Shambhavi Arya, Nampoothiri Sheela, Phadke Shubha |
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- Page last updated:Apr 22, 2024
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