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Journal Abstract Search

206 related items for PubMed ID: 23335808

  • 1. Deletions in 16q24.2 are associated with autism spectrum disorder, intellectual disability and congenital renal malformation.
    Handrigan GR, Chitayat D, Lionel AC, Pinsk M, Vaags AK, Marshall CR, Dyack S, Escobar LF, Fernandez BA, Stegman JC, Rosenfeld JA, Shaffer LG, Goodenberger M, Hodge JC, Cain JE, Babul-Hirji R, Stavropoulos DJ, Yiu V, Scherer SW, Rosenblum ND.
    J Med Genet; 2013 Mar; 50(3):163-73. PubMed ID: 23335808
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  • 4. Longitudinal follow-up of autism spectrum features and sensory behaviors in Angelman syndrome by deletion class.
    Peters SU, Horowitz L, Barbieri-Welge R, Taylor JL, Hundley RJ.
    J Child Psychol Psychiatry; 2012 Feb; 53(2):152-9. PubMed ID: 21831244
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  • 5. Phenotypic spectrum associated with de novo and inherited deletions and duplications at 16p11.2 in individuals ascertained for diagnosis of autism spectrum disorder.
    Fernandez BA, Roberts W, Chung B, Weksberg R, Meyn S, Szatmari P, Joseph-George AM, Mackay S, Whitten K, Noble B, Vardy C, Crosbie V, Luscombe S, Tucker E, Turner L, Marshall CR, Scherer SW.
    J Med Genet; 2010 Mar; 47(3):195-203. PubMed ID: 19755429
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  • 8. Molecular and clinical analyses of 16q24.1 duplications involving FOXF1 identify an evolutionarily unstable large minisatellite.
    Dharmadhikari AV, Gambin T, Szafranski P, Cao W, Probst FJ, Jin W, Fang P, Gogolewski K, Gambin A, George-Abraham JK, Golla S, Boidein F, Duban-Bedu B, Delobel B, Andrieux J, Becker K, Holinski-Feder E, Cheung SW, Stankiewicz P.
    BMC Med Genet; 2014 Dec 04; 15():128. PubMed ID: 25472632
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  • 10. Microcephaly, intellectual impairment, bilateral vesicoureteral reflux, distichiasis, and glomuvenous malformations associated with a 16q24.3 contiguous gene deletion and a Glomulin mutation.
    Butler MG, Dagenais SL, Garcia-Perez JL, Brouillard P, Vikkula M, Strouse P, Innis JW, Glover TW.
    Am J Med Genet A; 2012 Apr 04; 158A(4):839-49. PubMed ID: 22407726
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  • 14. Familial KANK1 deletion that does not follow expected imprinting pattern.
    Vanzo RJ, Martin MM, Sdano MR, South ST.
    Eur J Med Genet; 2013 May 04; 56(5):256-9. PubMed ID: 23454270
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  • 15. Chromosomal microarray analysis of consecutive individuals with autism spectrum disorders or learning disability presenting for genetic services.
    Roberts JL, Hovanes K, Dasouki M, Manzardo AM, Butler MG.
    Gene; 2014 Feb 01; 535(1):70-8. PubMed ID: 24188901
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  • 20. Identification of ANKRD11 and ZNF778 as candidate genes for autism and variable cognitive impairment in the novel 16q24.3 microdeletion syndrome.
    Willemsen MH, Fernandez BA, Bacino CA, Gerkes E, de Brouwer AP, Pfundt R, Sikkema-Raddatz B, Scherer SW, Marshall CR, Potocki L, van Bokhoven H, Kleefstra T.
    Eur J Hum Genet; 2010 Apr 01; 18(4):429-35. PubMed ID: 19920853
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