Citations for
1DEL7Q31, FOXP2
Mosaic 7q31 Deletion Involving FOXP2 Gene Associated With Language Impairment.
Palka C, Alfonsi M, Mohn A, Cerbo R, Franchi PG, Fantasia D, Morizio E, Stuppia L, Calabrese G, Zori R, Chiarelli F, Palka G.
Pediatrics 129(1):e183-8. Epub 2011 Dec 5. 2012
2DEL7Q31, FOXP2, SPCH1
Phenotype of FOXP2 haploinsufficiency in a mother and son.
Rice GM, Raca G, Jakielski KJ, Laffin JJ, Iyama-Kurtycz CM, Hartley SL, Sprague RE, Heintzelman AT, Shriberg LD.
Am J Med Genet A m J Med Genet A. 2011 Nov 21. doi: 10.1002/ajmg.a.34354. [Epub ahead of print] 2011
3DEL7Q31, SPCH1, AUTS9, FOXP2, WNT2
Deletion of 7q31.1 supports involvement of FOXP2 in language impairment: Clinical report and review.
Lennon PA, Cooper ML, Peiffer DA, Gunderson KL, Patel A, Peters S, Cheung SW, Bacino CA.
Am J Med Genet A [Epub ahead of print] 2007
4DEL7Q31, FOXP2, SPCH1
Speech and language impairment and oromotor dyspraxia due to deletion of 7q31 that involves FOXP2.
Zeesman S, Nowaczyk MJ, Teshima I, Roberts W, Cardy JO, Brian J, Senman L, Feuk L, Osborne LR, Scherer SW.
Am J Med Genet A 140(5):509-14. 2006
5FOXP2, DEL7Q31
Absence of a Paternally Inherited FOXP2 Gene in Developmental Verbal Dyspraxia.
Feuk L, Kalervo A, Lipsanen-Nyman M, Skaug J, Nakabayashi K, Finucane B, Hartung D, Innes M, Kerem B, Nowaczyk MJ, Rivlin J, Roberts W, Senman L, Summers A, Szatmari P, Wong V, Vincent JB, Zeesman S, Osborne LR, Cardy JO, Kere J, Scherer SW, Hannula-Jouppi K.
Am J Hum Genet 79(5):965-72. Epub 2006 Sep 27. 2006
6FOXP2, SPCH1, DEL7Q31
The SPCH1 region on human 7q31: genomic characterization of the critical interval and localization of translocations associated with speech and language disorder.
Lai CS, Fisher SE, Hurst JA, Levy ER, Hodgson S, Fox M, Jeremiah S, Povey S, Jamison DC, Green ED, Vargha-Khadem F, Monaco AP.
Am J Hum Genet 67(2):357-68. 2000