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23. 3p14.1 de novo microdeletion involving the FOXP1 gene in an adult patient with autism, severe speech delay and deficit of motor coordination. Palumbo O; D'Agruma L; Minenna AF; Palumbo P; Stallone R; Palladino T; Zelante L; Carella M Gene; 2013 Mar; 516(1):107-13. PubMed ID: 23287644 [TBL] [Abstract][Full Text] [Related]
24. Mitochondrial dysfunction and oxidative stress contribute to cognitive and motor impairment in FOXP1 syndrome. Wang J; Fröhlich H; Torres FB; Silva RL; Poschet G; Agarwal A; Rappold GA Proc Natl Acad Sci U S A; 2022 Feb; 119(8):. PubMed ID: 35165191 [TBL] [Abstract][Full Text] [Related]
25. Severe speech impairment is a distinguishing feature of FOXP1-related disorder. Braden RO; Amor DJ; Fisher SE; Mei C; Myers CT; Mefford H; Gill D; Srivastava S; Swanson LC; Goel H; Scheffer IE; Morgan AT Dev Med Child Neurol; 2021 Dec; 63(12):1417-1426. PubMed ID: 34109629 [TBL] [Abstract][Full Text] [Related]
26. Co-occurrence of mutations in FOXP1 and PTCH1 in a girl with extreme megalencephaly, callosal dysgenesis and profound intellectual disability. Zombor M; Kalmár T; Maróti Z; Zimmermann A; Máté A; Bereczki C; Sztriha L J Hum Genet; 2018 Nov; 63(11):1189-1193. PubMed ID: 30181650 [TBL] [Abstract][Full Text] [Related]
27. [I V. Vocal disturbances in neuro-psychiatric illnesses and in laryngeal paralyses (author's transl)]. Johannsen HS; Pascher W HNO; 1976 Jan; 24(1):20-7. PubMed ID: 955988 [TBL] [Abstract][Full Text] [Related]
28. Genetic abnormalities in FOXP1 are associated with congenital heart defects. Chang SW; Mislankar M; Misra C; Huang N; Dajusta DG; Harrison SM; McBride KL; Baker LA; Garg V Hum Mutat; 2013 Sep; 34(9):1226-30. PubMed ID: 23766104 [TBL] [Abstract][Full Text] [Related]
29. [Clinical features and genetic analysis of three children with mental retardation, language impairment and autistic features due to de novo variants of FOXP1 gene]. Hua R; Xu X; Wu D; Yang L; Yuan J; Zhu J Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2021 Dec; 38(12):1194-1198. PubMed ID: 34839505 [TBL] [Abstract][Full Text] [Related]
31. Aphonia due to vocal cord impairment induced by carbon monoxide poisoning. Koga S; Sadahiro T; Ito S; Asahina M; Oda S Acute Med Surg; 2014 Apr; 1(2):119-121. PubMed ID: 29930834 [TBL] [Abstract][Full Text] [Related]
32. Familial congenital bilateral vocal fold paralysis: a novel gene translocation. Hsu AK; Rosow DE; Wallerstein RJ; April MM Int J Pediatr Otorhinolaryngol; 2015 Mar; 79(3):323-7. PubMed ID: 25617187 [TBL] [Abstract][Full Text] [Related]
36. Gastrointestinal dysfunction in autism displayed by altered motility and achalasia in Fröhlich H; Kollmeyer ML; Linz VC; Stuhlinger M; Groneberg D; Reigl A; Zizer E; Friebe A; Niesler B; Rappold G Proc Natl Acad Sci U S A; 2019 Oct; 116(44):22237-22245. PubMed ID: 31611379 [TBL] [Abstract][Full Text] [Related]
37. FOXP1 syndrome: a review of the literature and practice parameters for medical assessment and monitoring. Lozano R; Gbekie C; Siper PM; Srivastava S; Saland JM; Sethuram S; Tang L; Drapeau E; Frank Y; Buxbaum JD; Kolevzon A J Neurodev Disord; 2021 Apr; 13(1):18. PubMed ID: 33892622 [TBL] [Abstract][Full Text] [Related]
38. Risk factors associated with prolonged intubation and laryngeal injury. Santos PM; Afrassiabi A; Weymuller EA Otolaryngol Head Neck Surg; 1994 Oct; 111(4):453-9. PubMed ID: 7936678 [TBL] [Abstract][Full Text] [Related]
39. 372 kb microdeletion in 18q12.3 causing SETBP1 haploinsufficiency associated with mild mental retardation and expressive speech impairment. Marseglia G; Scordo MR; Pescucci C; Nannetti G; Biagini E; Scandurra V; Gerundino F; Magi A; Benelli M; Torricelli F Eur J Med Genet; 2012 Mar; 55(3):216-21. PubMed ID: 22333924 [TBL] [Abstract][Full Text] [Related]
40. The distinct and overlapping phenotypic spectra of FOXP1 and FOXP2 in cognitive disorders. Bacon C; Rappold GA Hum Genet; 2012 Nov; 131(11):1687-98. PubMed ID: 22736078 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]