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Journal Abstract Search

1446 related items for PubMed ID: 23711909

  • 21. [Analysis of copy number variations in 66 children with unexplained mental retardation/developmental delay using chromosomal microarrays].
    Li Y, Qiu W, Ye J, Han L, Zhang H, Gu X.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Dec; 31(6):703-7. PubMed ID: 25449071
    [Abstract] [Full Text] [Related]

  • 22. Array CGH in patients with developmental delay or intellectual disability: are there phenotypic clues to pathogenic copy number variants?
    Shoukier M, Klein N, Auber B, Wickert J, Schröder J, Zoll B, Burfeind P, Bartels I, Alsat EA, Lingen M, Grzmil P, Schulze S, Keyser J, Weise D, Borchers M, Hobbiebrunken E, Röbl M, Gärtner J, Brockmann K, Zirn B.
    Clin Genet; 2013 Jan; 83(1):53-65. PubMed ID: 22283495
    [Abstract] [Full Text] [Related]

  • 23. 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
    [Abstract] [Full Text] [Related]

  • 24. Recurrent benign copy number variants & issues in interpretation of variants of unknown significance identified by cytogenetic microarray in Indian patients with intellectual disability.
    Boggula VR, Agarwal M, Kumar R, Awasthi S, Phadke SR.
    Indian J Med Res; 2015 Dec 01; 142(6):699-712. PubMed ID: 26831419
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  • 27. Chromosomal Aberrations in Pediatric Patients With Moderate/Severe Developmental Delay/Intellectual Disability With Abundant Phenotypic Heterogeneities: A Single-Center Study.
    Wu D, Wu Y, Lan Y, Lan S, Zhong Z, Li D, Zheng Z, Wang H, Ma L.
    Pediatr Neurol; 2023 Oct 01; 147():72-81. PubMed ID: 37566956
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  • 28. Chromosomal microarray testing influences medical management.
    Coulter ME, Miller DT, Harris DJ, Hawley P, Picker J, Roberts AE, Sobeih MM, Irons M.
    Genet Med; 2011 Sep 01; 13(9):770-6. PubMed ID: 21716121
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  • 29. Phenotype comparison among individuals with developmental delay/intellectual disability with or without genomic imbalances.
    de Souza LC, Dos Santos AP, Sgardioli IC, Viguetti-Campos NL, Marques Prota JR, de Oliveira-Sobrinho RP, Vieira TP, Gil-da-Silva-Lopes VL.
    J Intellect Disabil Res; 2019 Nov 01; 63(11):1379-1389. PubMed ID: 30900361
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  • 30. Copy number variants analysis in a cohort of isolated and syndromic developmental delay/intellectual disability reveals novel genomic disorders, position effects and candidate disease genes.
    Di Gregorio E, Riberi E, Belligni EF, Biamino E, Spielmann M, Ala U, Calcia A, Bagnasco I, Carli D, Gai G, Giordano M, Guala A, Keller R, Mandrile G, Arduino C, Maffè A, Naretto VG, Sirchia F, Sorasio L, Ungari S, Zonta A, Zacchetti G, Talarico F, Pappi P, Cavalieri S, Giorgio E, Mancini C, Ferrero M, Brussino A, Savin E, Gandione M, Pelle A, Giachino DF, De Marchi M, Restagno G, Provero P, Cirillo Silengo M, Grosso E, Buxbaum JD, Pasini B, De Rubeis S, Brusco A, Ferrero GB.
    Clin Genet; 2017 Oct 01; 92(4):415-422. PubMed ID: 28295210
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  • 31. Chromosomal microarray analysis in developmental delay and intellectual disability with comorbid conditions.
    Fan Y, Wu Y, Wang L, Wang Y, Gong Z, Qiu W, Wang J, Zhang H, Ji X, Ye J, Han L, Jin X, Shen Y, Li F, Xiao B, Liang L, Zhang X, Liu X, Gu X, Yu Y.
    BMC Med Genomics; 2018 May 24; 11(1):49. PubMed ID: 29793483
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  • 32. Genetic profile and clinical application of chromosomal microarray in children with intellectual disability in Hong Kong.
    Chan PY, Luk HM, Lee FM, Lo IF.
    Hong Kong Med J; 2018 Oct 24; 24(5):451-459. PubMed ID: 30262673
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  • 33. [The diagnostic value of chromosome microarray analysis technique in the genetic causes of children with intellectual disability or global developmental delay].
    Wu HR, Li L, Ma YN, Liu CL, Pei P, Zheng XF, Wang ST, Xiao Y, Bu DF, Xu YF, Pan H, Qi Y.
    Zhonghua Yi Xue Za Zhi; 2021 Jan 19; 101(3):224-228. PubMed ID: 33455150
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  • 34. A cohort study of neurodevelopmental disorders and/or congenital anomalies using high resolution chromosomal microarrays in southern Brazil highlighting the significance of ASD.
    Chaves TF, Ocampos M, Barbato IT, de Camargo Pinto LL, de Luca GR, Barbato Filho JH, Bernardi P, Costa Netto Muniz Y, Francesca Maris A.
    Sci Rep; 2024 Feb 14; 14(1):3762. PubMed ID: 38355898
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  • 35. Updates in the genetic evaluation of the child with global developmental delay or intellectual disability.
    Flore LA, Milunsky JM.
    Semin Pediatr Neurol; 2012 Dec 14; 19(4):173-80. PubMed ID: 23245550
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  • 37. Array-CGH analysis in patients with intellectual disability and/or congenital malformations in Brazil.
    Vianna GS, Medeiros PF, Alves AF, Silva TO, Jehee FS.
    Genet Mol Res; 2016 Feb 19; 15(1):. PubMed ID: 26909975
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  • 39. [Molecular diagnosis of children with unexplained intellectual disability/ developmental delay by array-CGH].
    He XY, Chen XC, Li R, Li P, Lu AM.
    Zhongguo Dang Dai Er Ke Za Zhi; 2015 May 19; 17(5):459-63. PubMed ID: 26014695
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