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6. GPSM2 mutations in Chudley-McCullough syndrome. Diaz-Horta O; Sirmaci A; Doherty D; Nance W; Arnos K; Pandya A; Tekin M Am J Med Genet A; 2012 Nov; 158A(11):2972-3. PubMed ID: 22987632 [No Abstract] [Full Text] [Related]
7. Brothers with Chudley-McCullough syndrome: sensorineural deafness, agenesis of the corpus callosum, and other structural brain abnormalities. Østergaard E; Pedersen VF; Skriver EB; Brøndum-Nielsen K Am J Med Genet A; 2004 Jan; 124A(1):74-8. PubMed ID: 14679590 [TBL] [Abstract][Full Text] [Related]
8. Cochlear implantation in a 16-month-old with Chudley-McCullough Syndrome. Kalil G; Barrera S; Elkins A; Grillis A; Carron J Am J Otolaryngol; 2022; 43(4):103487. PubMed ID: 35569212 [TBL] [Abstract][Full Text] [Related]
9. GPSM2 mutations cause the brain malformations and hearing loss in Chudley-McCullough syndrome. Doherty D; Chudley AE; Coghlan G; Ishak GE; Innes AM; Lemire EG; Rogers RC; Mhanni AA; Phelps IG; Jones SJ; Zhan SH; Fejes AP; Shahin H; Kanaan M; Akay H; Tekin M; ; Triggs-Raine B; Zelinski T Am J Hum Genet; 2012 Jun; 90(6):1088-93. PubMed ID: 22578326 [TBL] [Abstract][Full Text] [Related]
10. Chudley-McCullough Syndrome: Variable Clinical Picture in Twins with a Novel GPSM2 Mutation. Koenigstein K; Gramsch C; Kolodziej M; Neubauer BA; Weber A; Lechner S; Hahn A Neuropediatrics; 2016 Jun; 47(3):197-201. PubMed ID: 27064331 [TBL] [Abstract][Full Text] [Related]
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12. Cochlear implant in a subject affected by the Chudley-McCullough Syndrome. Forli F; Fiacchini G; Bruschini L; Caniglia M; Berrettini S Cochlear Implants Int; 2019 Jul; 20(4):217-221. PubMed ID: 30907716 [No Abstract] [Full Text] [Related]
13. Intracranial cystic lesions and polydactyly associated with acrocallosal syndrome: Sonographic findings in two cases. Mohanty HS; Shirodkar KK; Sharma N; Bind MK; Nandikoor S J Clin Ultrasound; 2019 Oct; 47(8):497-500. PubMed ID: 31318057 [TBL] [Abstract][Full Text] [Related]
14. Neuroimaging Findings in a Child With SensorineuralHearing Loss. Samanta D; Ramakrishnaiah R Pediatr Neurol; 2018 Nov; 88():75-76. PubMed ID: 30327240 [No Abstract] [Full Text] [Related]
15. Sensorineural deafness, hydrocephalus and structural brain abnormalities in two sisters: the Chudley-McCullough syndrome. Matteucci F; Tarantino E; Bianchi MC; Cingolani C; Fattori B; Nacci A; Ursino F Am J Med Genet A; 2006 Jun; 140(11):1183-8. PubMed ID: 16642503 [TBL] [Abstract][Full Text] [Related]
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18. Spectrum of the acrocallosal syndrome. Koenig R; Bach A; Woelki U; Grzeschik KH; Fuchs S Am J Med Genet; 2002 Feb; 108(1):7-11. PubMed ID: 11857542 [TBL] [Abstract][Full Text] [Related]
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20. Commissural malformations: beyond the corpus callosum. Smith T; Tekes A; Boltshauser E; Huisman TA J Neuroradiol; 2008 Dec; 35(5):301-3. PubMed ID: 18692242 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]