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Journal Abstract Search

347 related items for PubMed ID: 24300712

  • 41. Chromosomal Microarray With Clinical Diagnostic Utility in Children With Developmental Delay or Intellectual Disability.
    Lee JS, Hwang H, Kim SY, Kim KJ, Choi JS, Woo MJ, Choi YM, Jun JK, Lim BC, Chae JH.
    Ann Lab Med; 2018 Sep; 38(5):473-480. PubMed ID: 29797819
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  • 42. [Value of copy number variation analysis and chromosomal karyotyping for the diagnosis of children with intellectual disability/developmental delay].
    Lin M, Xue H, Wang Y, Huang H, Fu M, Guo N, Xu L.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2021 Mar 10; 38(3):228-231. PubMed ID: 33751530
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  • 44. Genomic study via chromosomal microarray analysis in a group of Romanian patients with obesity and developmental disability/intellectual disability.
    Micleaa D, Al-Khzouza C, Osan S, Bucerzan S, Cret V, Popp RA, Puiu M, Chirita-Emandi A, Zimbru C, Ghervan C.
    J Pediatr Endocrinol Metab; 2019 Jul 26; 32(7):667-674. PubMed ID: 31150357
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  • 45. Appropriateness of array-CGH in the ADHD clinics: A comparative study.
    Baccarin M, Picinelli C, Tomaiuolo P, Castronovo P, Costa A, Verdecchia M, Cannizzaro C, Barbieri G, Sacco R, Persico AM, Lintas C.
    Genes Brain Behav; 2020 Jul 26; 19(6):e12651. PubMed ID: 32141190
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  • 46. Clinical significance of rare copy number variations in epilepsy: a case-control survey using microarray-based comparative genomic hybridization.
    Striano P, Coppola A, Paravidino R, Malacarne M, Gimelli S, Robbiano A, Traverso M, Pezzella M, Belcastro V, Bianchi A, Elia M, Falace A, Gazzerro E, Ferlazzo E, Freri E, Galasso R, Gobbi G, Molinatto C, Cavani S, Zuffardi O, Striano S, Ferrero GB, Silengo M, Cavaliere ML, Benelli M, Magi A, Piccione M, Dagna Bricarelli F, Coviello DA, Fichera M, Minetti C, Zara F.
    Arch Neurol; 2012 Mar 26; 69(3):322-30. PubMed ID: 22083797
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  • 48. Experience of chromosomal microarray applied in prenatal and postnatal settings in Hong Kong.
    Cheng SSW, Chan KYK, Leung KKP, Au PKC, Tam WK, Li SKM, Luk HM, Kan ASY, Chung BHY, Lo IFM, Tang MHY.
    Am J Med Genet C Semin Med Genet; 2019 Jun 26; 181(2):196-207. PubMed ID: 30903683
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  • 49. Copy number variation findings among 50 children and adolescents with autism spectrum disorder.
    Sorte HS, Gjevik E, Sponheim E, Eiklid KL, Rødningen OK.
    Psychiatr Genet; 2013 Apr 26; 23(2):61-9. PubMed ID: 23277134
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  • 51. Customized high resolution CGH-array for clinical diagnosis reveals additional genomic imbalances in previous well-defined pathological samples.
    Vallespín E, Palomares Bralo M, Mori MÁ, Martín R, García-Miñaúr S, Fernández L, de Torres ML, García-Santiago F, Mansilla E, Santos F, M-Montaño VE, Crespo MC, Martín S, Martínez-Glez V, Delicado A, Lapunzina P, Nevado J.
    Am J Med Genet A; 2013 Aug 26; 161A(8):1950-60. PubMed ID: 23798500
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  • 52. The Diagnostic Yield of Array Comparative Genomic Hybridization Is High Regardless of Severity of Intellectual Disability/Developmental Delay in Children.
    D'Arrigo S, Gavazzi F, Alfei E, Zuffardi O, Montomoli C, Corso B, Buzzi E, Sciacca FL, Bulgheroni S, Riva D, Pantaleoni C.
    J Child Neurol; 2016 May 26; 31(6):691-9. PubMed ID: 26511719
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  • 58. A discovery resource of rare copy number variations in individuals with autism spectrum disorder.
    Prasad A, Merico D, Thiruvahindrapuram B, Wei J, Lionel AC, Sato D, Rickaby J, Lu C, Szatmari P, Roberts W, Fernandez BA, Marshall CR, Hatchwell E, Eis PS, Scherer SW.
    G3 (Bethesda); 2012 Dec 26; 2(12):1665-85. PubMed ID: 23275889
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  • 59. 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 26; 47(3):195-203. PubMed ID: 19755429
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