BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

132 related articles for article (PubMed ID: 25893121)

  • 1. Case of 7p22.1 Microduplication Detected by Whole Genome Microarray (REVEAL) in Workup of Child Diagnosed with Autism.
    Goitia V; Oquendo M; Stratton R
    Case Rep Genet; 2015; 2015():212436. PubMed ID: 25893121
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Clinical and molecular characterization of a second case of 7p22.1 microduplication.
    Preiksaitiene E; Kasnauskiene J; Ciuladaite Z; Tumiene B; Patsalis PC; Kučinskas V
    Am J Med Genet A; 2012 May; 158A(5):1200-3. PubMed ID: 22495914
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Refinement of the critical 7p22.1 deletion region: Haploinsufficiency of ACTB is the cause of the 7p22.1 microdeletion-related developmental disorders.
    Palumbo O; Accadia M; Palumbo P; Leone MP; Scorrano A; Palladino T; Stallone R; Bonaglia MC; Carella M
    Eur J Med Genet; 2018 May; 61(5):248-252. PubMed ID: 29274487
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 7p22.1 microduplication syndrome: Refinement of the critical region.
    Ronzoni L; Grassi FS; Pezzani L; Tucci A; Baccarin M; Esposito S; Milani D
    Eur J Med Genet; 2017 Feb; 60(2):114-117. PubMed ID: 27866048
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Clinical and molecular characterization of chromosome 7p22.1 microduplication detected by array CGH.
    Chui JV; Weisfeld-Adams JD; Tepperberg J; Mehta L
    Am J Med Genet A; 2011 Oct; 155A(10):2508-11. PubMed ID: 21998864
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 7p22.1 microduplication syndrome: Clinical and molecular characterization of an adult case and review of the literature.
    Caselli R; Ballarati L; Vignoli A; Peron A; Recalcati MP; Catusi I; Larizza L; Giardino D
    Eur J Med Genet; 2015 Nov; 58(11):578-83. PubMed ID: 26297194
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A Case of the 7p22.2 Microduplication: Refinement of the Critical Chromosome Region for 7p22 Duplication Syndrome.
    Cox DM; Butler MG
    J Pediatr Genet; 2015 Mar; 4(1):34-7. PubMed ID: 27617114
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 7p22.1 microdeletions involving ACTB associated with developmental delay, short stature, and microcephaly.
    Shimojima K; Narai S; Togawa M; Doumoto T; Sangu N; Vanakker OM; de Paepe A; Edwards M; Whitehall J; Brescianini S; Petit F; Andrieux J; Yamamoto T
    Eur J Med Genet; 2016 Oct; 59(10):502-6. PubMed ID: 27633570
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 7p22.2 Microduplication: A Pathogenic CNV?
    Bauleo A; Montesanto A; Pace V; Guarasci F; Apa R; Brando R; De Stefano L; Sestito S; Concolino D; Falcone E
    Genes (Basel); 2023 Jun; 14(6):. PubMed ID: 37372471
    [TBL] [Abstract][Full Text] [Related]  

  • 10. De Novo Duplication of 7p21.1p22.2 in a Child with Autism Spectrum Disorder and Craniofacial Dysmorphism.
    Udayakumar AM; Al-Mamari W; Al-Sayegh A; Al-Kindy A
    Sultan Qaboos Univ Med J; 2015 Aug; 15(3):e415-9. PubMed ID: 26357560
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Case report: 7p22.3 deletion and 8q24.3 duplication in a patient with epilepsy and psychomotor delay-Does both possibly act to modulate a candidate gene region for the patient's phenotype?
    Touhami R; Foddha H; Alix E; Jalloul A; Mougou-Zerelli S; Saad A; Sanlaville D; Haj Khelil A
    Front Genet; 2022; 13():1061539. PubMed ID: 36778913
    [No Abstract]   [Full Text] [Related]  

  • 12. 3q29 microduplication syndrome: New evidence for the refinement of the critical region.
    Bauleo A; Pace V; Montesanto A; De Stefano L; Brando R; Puntorieri D; Cento L; Genuardi M; Falcone E
    Mol Genet Genomic Med; 2023 Apr; 11(4):e2130. PubMed ID: 36691815
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Prenatal diagnosis of partial monosomy 5p (5p15.1→pter) and partial trisomy 7p (7p15.2→pter) associated with cystic hygroma, abnormal skull development, and ventriculomegaly.
    Chen CP; Wang LK; Chern SR; Wu PS; Ko K; Chen YN; Chen SW; Lee MS; Wang W
    Taiwan J Obstet Gynecol; 2016 Aug; 55(4):591-5. PubMed ID: 27590389
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Phenotypic spectrum of interstitial 7p duplication in mosaic and non-mosaic forms.
    Cox H; Stewart H; Hall L; Donnai D
    Am J Med Genet; 2002 May; 109(4):306-10. PubMed ID: 11992485
    [TBL] [Abstract][Full Text] [Related]  

  • 15.
    Gug C; Stoicanescu D; Mozos I; Nussbaum L; Cevei M; Stambouli D; Pavel AG; Doros G
    Front Pediatr; 2020; 8():375. PubMed ID: 32733829
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Exploring the 7p22.1 chromosome as a candidate region for autism.
    Bayou N; Belhadj A; Daoud H; Briault S; Helayem MB; Chaabouni H; M'rad R
    J Biomed Biotechnol; 2010; 2010():423894. PubMed ID: 20414355
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Clinical and genetic analysis of a case carrying 7p22.3 deletion, 7p22.3p22.2 duplication and 7q33q36.3 duplication].
    Shen N; Guo R; Liu Y; Gai Z
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 Jul; 36(7):708-711. PubMed ID: 31302917
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Report of a patient and further clinical and molecular characterization of interstitial 4p16.3 microduplication.
    Palumbo O; Palumbo P; Ferri E; Riviello FN; Cloroformio L; Carella M; Di Giacomo MC
    Mol Cytogenet; 2015; 8():15. PubMed ID: 25774220
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Novel microduplication of CHL1 gene in a patient with autism spectrum disorder: a case report and a brief literature review.
    Li C; Liu C; Zhou B; Hu C; Xu X
    Mol Cytogenet; 2016; 9():51. PubMed ID: 27354858
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 17q23.2q23.3 de novo duplication in association with speech and language disorder, learning difficulties, incoordination, motor skill impairment, and behavioral disturbances: a case report.
    Wessel K; Suleiman J; Khalaf TE; Kishore S; Rolfs A; El-Hattab AW
    BMC Med Genet; 2017 Oct; 18(1):119. PubMed ID: 29070031
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.