These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

142 related articles for article (PubMed ID: 25193415)

  • 1. 3p interstitial deletion including PRICKLE2 in identical twins with autistic features.
    Okumura A; Yamamoto T; Miyajima M; Shimojima K; Kondo S; Abe S; Ikeno M; Shimizu T
    Pediatr Neurol; 2014 Nov; 51(5):730-3. PubMed ID: 25193415
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Autism multiplex family with 16p11.2p12.2 microduplication syndrome in monozygotic twins and distal 16p11.2 deletion in their brother.
    Tabet AC; Pilorge M; Delorme R; Amsellem F; Pinard JM; Leboyer M; Verloes A; Benzacken B; Betancur C
    Eur J Hum Genet; 2012 May; 20(5):540-6. PubMed ID: 22234155
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A 3p interstitial deletion in two monozygotic twin brothers and an 18-year-old man: further characterization and review.
    Schwaibold EM; Zoll B; Burfeind P; Hobbiebrunken E; Wilken B; Funke R; Shoukier M
    Am J Med Genet A; 2013 Oct; 161A(10):2634-40. PubMed ID: 23949945
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 3p14 De Novo Interstitial Microdeletion in a Patient with Intellectual Disability and Autistic Features with Language Impairment: A Comparison with Similar Cases.
    de la Hoz AB; Maortua H; García-Rives A; Martínez-González MJ; Ezquerra M; Tejada MI
    Case Rep Genet; 2015; 2015():876348. PubMed ID: 26075115
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Identification of a novel deletion region in 3q29 microdeletion syndrome by oligonucleotide array comparative genomic hybridization].
    Seo EJ; Jun KR; Yoo HW; Yoo HK; Lee JO
    Korean J Lab Med; 2010 Feb; 30(1):70-5. PubMed ID: 20197726
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A variant Cri du Chat phenotype and autism spectrum disorder in a subject with de novo cryptic microdeletions involving 5p15.2 and 3p24.3-25 detected using whole genomic array CGH.
    Harvard C; Malenfant P; Koochek M; Creighton S; Mickelson EC; Holden JJ; Lewis ME; Rajcan-Separovic E
    Clin Genet; 2005 Apr; 67(4):341-51. PubMed ID: 15733271
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A 1.37-Mb 12p11.22-p11.21 deletion coincident with a 367-kb 22q11.2 duplication detected by array comparative genomic hybridization in an adolescent girl with autism and difficulty in self-care of menstruation.
    Chen CP; Lin SP; Chern SR; Wu PS; Su JW; Lee CC; Wang W
    Taiwan J Obstet Gynecol; 2014 Mar; 53(1):74-8. PubMed ID: 24767651
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Developmental delay and facial dysmorphism in a child with an 8.9 Mb de novo interstitial deletion of 3q25.1-q25.32: Genotype-phenotype correlations of chromosome 3q25 deletion syndrome.
    Moortgat S; Verellen-Dumoulin C; Maystadt I; Parmentier B; Grisart B; Hennecker JL; Destree A
    Eur J Med Genet; 2011; 54(2):177-80. PubMed ID: 21167329
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Clinical findings in cases with 9q deletion encompassing the 9q21.11q21.32 region.
    Tuğ E; Ergün MA; Perçin EF
    Turk J Pediatr; 2018; 60(1):94-98. PubMed ID: 30102487
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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; 167A(12):3121-9. PubMed ID: 26332054
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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; 152A(10):2459-67. PubMed ID: 20830797
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 9q31.1q31.3 deletion in two patients with similar clinical features: a newly recognized microdeletion syndrome?
    Mucciolo M; Magini P; Marozza A; Mongelli P; Mencarelli MA; Hayek G; Tavalazzi F; Mari F; Seri M; Renieri A; Graziano C
    Am J Med Genet A; 2014 Mar; 164A(3):685-90. PubMed ID: 24376033
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Clinical and molecular cytogenetic characterisation of a newly recognised microdeletion syndrome involving 2p15-16.1.
    Rajcan-Separovic E; Harvard C; Liu X; McGillivray B; Hall JG; Qiao Y; Hurlburt J; Hildebrand J; Mickelson EC; Holden JJ; Lewis ME
    J Med Genet; 2007 Apr; 44(4):269-76. PubMed ID: 16963482
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Monozygotic twins discordant for submicroscopic chromosomal anomalies in 2p25.3 region detected by array CGH.
    Rio M; Royer G; Gobin S; de Blois MC; Ozilou C; Bernheim A; Nizon M; Munnich A; Bonnefont JP; Romana S; Vekemans M; Turleau C; Malan V
    Clin Genet; 2013 Jul; 84(1):31-6. PubMed ID: 23061379
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Report of trisomy 2q34-qter and monosomy 4q35.2-qter in a child with mild dysmorphic syndrome and karyotype 46,XY,der(4)t(2;4)(q34;q35.2)pat.
    Meza-Espinoza JP; Sáinz González E; León-León CJN; Arámbula-Meraz E; Contreras-Gutiérrez JA; García-Magallanes N; Madueña-Molina J; Luque-Ortega F; Cervín-Serrano S; Picos-Cárdenas VJ
    Mol Cytogenet; 2020; 13():17. PubMed ID: 32467733
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 3p interstitial deletion: novel case report and review.
    Ţuţulan-Cunită AC; Papuc SM; Arghir A; Rötzer KM; Deshpande C; Lungeanu A; Budişteanu M
    J Child Neurol; 2012 Aug; 27(8):1062-6. PubMed ID: 22290856
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Deletion 2q37.3 and autism: molecular cytogenetic mapping of the candidate region for autistic disorder.
    Lukusa T; Vermeesch JR; Holvoet M; Fryns JP; Devriendt K
    Genet Couns; 2004; 15(3):293-301. PubMed ID: 15517821
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The proximal chromosome 14q microdeletion syndrome: delineation of the phenotype using high resolution SNP oligonucleotide microarray analysis (SOMA) and review of the literature.
    Torgyekes E; Shanske AL; Anyane-Yeboa K; Nahum O; Pirzadeh S; Blumfield E; Jobanputra V; Warburton D; Levy B
    Am J Med Genet A; 2011 Aug; 155A(8):1884-96. PubMed ID: 21744488
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Narrowing of the responsible region for severe developmental delay and autistic behaviors in WAGR syndrome down to 1.6 Mb including PAX6, WT1, and PRRG4.
    Yamamoto T; Togawa M; Shimada S; Sangu N; Shimojima K; Okamoto N
    Am J Med Genet A; 2014 Mar; 164A(3):634-8. PubMed ID: 24357251
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 3p14.1 de novo microdeletion involving the FOXP1 gene in an adult patient with autism, severe speech delay and deficit of motor coordination.
    Palumbo O; D'Agruma L; Minenna AF; Palumbo P; Stallone R; Palladino T; Zelante L; Carella M
    Gene; 2013 Mar; 516(1):107-13. PubMed ID: 23287644
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.