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217 related items for PubMed ID: 24214349

  • 1. 3q29 microdeletion syndrome: Cognitive and behavioral phenotype in four patients.
    Città S, Buono S, Greco D, Barone C, Alfei E, Bulgheroni S, Usilla A, Pantaleoni C, Romano C.
    Am J Med Genet A; 2013 Dec; 161A(12):3018-22. PubMed ID: 24214349
    [Abstract] [Full Text] [Related]

  • 2. Study protocol for The Emory 3q29 Project: evaluation of neurodevelopmental, psychiatric, and medical symptoms in 3q29 deletion syndrome.
    Murphy MM, Lindsey Burrell T, Cubells JF, España RA, Gambello MJ, Goines KCB, Klaiman C, Li L, Novacek DM, Papetti A, Sanchez Russo RL, Saulnier CA, Shultz S, Walker E, Mulle JG.
    BMC Psychiatry; 2018 Jun 08; 18(1):183. PubMed ID: 29884173
    [Abstract] [Full Text] [Related]

  • 3. Familial inheritance of the 3q29 microdeletion syndrome: case report and review.
    Khan WA, Cohen N, Scott SA, Pereira EM.
    BMC Med Genomics; 2019 Mar 18; 12(1):51. PubMed ID: 30885185
    [Abstract] [Full Text] [Related]

  • 4. Autistic and psychiatric findings associated with the 3q29 microdeletion syndrome: case report and review.
    Quintero-Rivera F, Sharifi-Hannauer P, Martinez-Agosto JA.
    Am J Med Genet A; 2010 Oct 18; 152A(10):2459-67. PubMed ID: 20830797
    [Abstract] [Full Text] [Related]

  • 5. Comprehensive phenotyping of neuropsychiatric traits in a multiplex 3q29 deletion family: a case report.
    Murphy MM, Burrell TL, Cubells JF, Epstein MT, Espana R, Gambello MJ, Goines K, Klaiman C, Koh S, Russo RS, Saulnier CA, Walker E, Emory 3q29 Project, Mulle JG.
    BMC Psychiatry; 2020 Apr 22; 20(1):184. PubMed ID: 32321479
    [Abstract] [Full Text] [Related]

  • 6. Psychiatric-disorder-related behavioral phenotypes and cortical hyperactivity in a mouse model of 3q29 deletion syndrome.
    Baba M, Yokoyama K, Seiriki K, Naka Y, Matsumura K, Kondo M, Yamamoto K, Hayashida M, Kasai A, Ago Y, Nagayasu K, Hayata-Takano A, Takahashi A, Yamaguchi S, Mori D, Ozaki N, Yamamoto T, Takuma K, Hashimoto R, Hashimoto H, Nakazawa T.
    Neuropsychopharmacology; 2019 Nov 22; 44(12):2125-2135. PubMed ID: 31216562
    [Abstract] [Full Text] [Related]

  • 7. 3q29 Microdeletion: a mental retardation disorder unassociated with a recognizable phenotype in two mother-daughter pairs.
    Digilio MC, Bernardini L, Mingarelli R, Capolino R, Capalbo A, Giuffrida MG, Versacci P, Novelli A, Dallapiccola B.
    Am J Med Genet A; 2009 Aug 22; 149A(8):1777-81. PubMed ID: 19610115
    [Abstract] [Full Text] [Related]

  • 8. Paroxysmal oculogyric dystonia associated with a de novo 3q29 microdeletion.
    Kaur H, Thom RP, Neumeyer AM, Bilancia CG, Wray SH, McDougle CJ.
    Psychiatr Genet; 2020 Aug 22; 30(4):119-123. PubMed ID: 32459710
    [Abstract] [Full Text] [Related]

  • 9. Neuropsychiatric phenotypes and a distinct constellation of ASD features in 3q29 deletion syndrome: results from the 3q29 registry.
    Pollak RM, Murphy MM, Epstein MP, Zwick ME, Klaiman C, Saulnier CA, Emory 3q29 Project, Mulle JG.
    Mol Autism; 2019 Aug 22; 10():30. PubMed ID: 31346402
    [Abstract] [Full Text] [Related]

  • 10. A novel 3q29 deletion associated with autism, intellectual disability, psychiatric disorders, and obesity.
    Biamino E, Di Gregorio E, Belligni EF, Keller R, Riberi E, Gandione M, Calcia A, Mancini C, Giorgio E, Cavalieri S, Pappi P, Talarico F, Fea AM, De Rubeis S, Cirillo Silengo M, Ferrero GB, Brusco A.
    Am J Med Genet B Neuropsychiatr Genet; 2016 Mar 22; 171B(2):290-9. PubMed ID: 26620927
    [Abstract] [Full Text] [Related]

  • 11. Neuropsychiatric phenotype in relation to gene variants in the hemizygous allele in 3q29 deletion carriers: A case series.
    Malt EA, Juhasz K, Frengen A, Wangensteen T, Emilsen NM, Hansen B, Agafonov O, Nilsen HL.
    Mol Genet Genomic Med; 2019 Sep 22; 7(9):e889. PubMed ID: 31347308
    [Abstract] [Full Text] [Related]

  • 12. Familial 3q29 microdeletion syndrome providing further evidence of involvement of the 3q29 region in bipolar disorder.
    Clayton-Smith J, Giblin C, Smith RA, Dunn C, Willatt L.
    Clin Dysmorphol; 2010 Jul 22; 19(3):128-132. PubMed ID: 20453639
    [Abstract] [Full Text] [Related]

  • 13. A clinical case report and literature review of the 3q29 microdeletion syndrome.
    Cox DM, Butler MG.
    Clin Dysmorphol; 2015 Jul 22; 24(3):89-94. PubMed ID: 25714563
    [Abstract] [Full Text] [Related]

  • 14. Novel features of 3q29 deletion syndrome: Results from the 3q29 registry.
    Glassford MR, Rosenfeld JA, Freedman AA, Zwick ME, Mulle JG, Unique Rare Chromosome Disorder Support Group.
    Am J Med Genet A; 2016 Apr 22; 170A(4):999-1006. PubMed ID: 26738761
    [Abstract] [Full Text] [Related]

  • 15. New phenotypes associated with 3q29 duplication syndrome: Results from the 3q29 registry.
    Pollak RM, Zinsmeister MC, Murphy MM, Zwick ME, Emory 3q29 Project, Mulle JG.
    Am J Med Genet A; 2020 May 22; 182(5):1152-1166. PubMed ID: 32154651
    [Abstract] [Full Text] [Related]

  • 16. Female patient with autistic disorder, intellectual disability, and co-morbid anxiety disorder: Expanding the phenotype associated with the recurrent 3q13.2-q13.31 microdeletion.
    Quintela I, Gomez-Guerrero L, Fernandez-Prieto M, Resches M, Barros F, Carracedo A.
    Am J Med Genet A; 2015 Dec 22; 167A(12):3121-9. PubMed ID: 26332054
    [Abstract] [Full Text] [Related]

  • 17. 1.3 Mb de novo deletion in chromosome band 3q29 associated with normal intelligence in a child.
    Cobb W, Anderson A, Turner C, Hoffman RD, Schonberg S, Levin SW.
    Eur J Med Genet; 2010 Dec 22; 53(6):415-8. PubMed ID: 20832509
    [Abstract] [Full Text] [Related]

  • 18. Further insight into the neurobehavioral pattern of children carrying the 2p16.3 heterozygous deletion involving NRXN1: Report of five new cases.
    Alfieri P, Scibelli F, Sinibaldi L, Valeri G, Caciolo C, Novello RL, Novelli A, Digilio MC, Tartaglia M, Vicari S.
    Genes Brain Behav; 2020 Sep 22; 19(7):e12687. PubMed ID: 32658356
    [Abstract] [Full Text] [Related]

  • 19. [Molecular characterisation and phenotypic description of two patients with reciprocal chromosomal aberrations in the region of the 3q29 microdeletion/microduplication syndromes].
    Quintela I, Barros-Angueira F, Perez-Gay L, Dacruz D, Castro-Gago M, Carracedo A, Eiris-Punal J.
    Rev Neurol; 2015 Sep 16; 61(6):255-60. PubMed ID: 26350776
    [Abstract] [Full Text] [Related]

  • 20. The 3q29 microdeletion syndrome: report of three new unrelated patients and in silico "RNA binding" analysis of the 3q29 region.
    Dasouki MJ, Lushington GH, Hovanes K, Casey J, Gorre M.
    Am J Med Genet A; 2011 Jul 16; 155A(7):1654-60. PubMed ID: 21626679
    [Abstract] [Full Text] [Related]

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