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 *

298 related articles for article (PubMed ID: 20688202)

  • 1. An emerging phenotype of proximal 11q deletions.
    Melis D; Genesio R; Cozzolino M; Del Giudice E; Mormile A; Imperati F; Ronga V; Della Casa R; Nitsch L; Andria G
    Eur J Med Genet; 2010; 53(5):340-3. PubMed ID: 20688202
    [TBL] [Abstract][Full Text] [Related]  

  • 2. De novo deletion of chromosome 11q13.4-q14.3 in a boy with microcephaly, ptosis and developmental delay.
    Wincent J; Schoumans J; Anderlid BM
    Eur J Med Genet; 2010; 53(1):50-3. PubMed ID: 19857611
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Identification of proximal 1p36 deletions using array-CGH: a possible new syndrome.
    Kang SH; Scheffer A; Ou Z; Li J; Scaglia F; Belmont J; Lalani SR; Roeder E; Enciso V; Braddock S; Buchholz J; Vacha S; Chinault AC; Cheung SW; Bacino CA
    Clin Genet; 2007 Oct; 72(4):329-38. PubMed ID: 17850629
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Interstitial deletion of 18q: comparative genomic hybridization array analysis of 46, XX,del(18)(q21.2.q21.33).
    Kato Z; Morimoto W; Kimura T; Matsushima A; Kondo N
    Birth Defects Res A Clin Mol Teratol; 2010 Feb; 88(2):132-5. PubMed ID: 19813260
    [TBL] [Abstract][Full Text] [Related]  

  • 5. An interstitial deletion of 7.1Mb in chromosome band 6p22.3 associated with developmental delay and dysmorphic features including heart defects, short neck, and eye abnormalities.
    Bremer A; Schoumans J; Nordenskjöld M; Anderlid BM; Giacobini M
    Eur J Med Genet; 2009; 52(5):358-62. PubMed ID: 19576304
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Proximal interstitial 1p36 deletion syndrome: the most proximal 3.5-Mb microdeletion identified on a dysmorphic and mentally retarded patient with inv(3)(p14.1q26.2).
    Shimojima K; Páez MT; Kurosawa K; Yamamoto T
    Brain Dev; 2009 Sep; 31(8):629-33. PubMed ID: 18835671
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Interstitial deletions of chromosome 6q: genotype-phenotype correlation utilizing array CGH.
    Klein OD; Cotter PD; Moore MW; Zanko A; Gilats M; Epstein CJ; Conte F; Rauen KA
    Clin Genet; 2007 Mar; 71(3):260-6. PubMed ID: 17309649
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. 11q- syndrome: three cases and a review of the literature.
    Leegte B; Kerstjens-Frederikse WS; Deelstra K; Begeer JH; van Essen AJ
    Genet Couns; 1999; 10(3):305-13. PubMed ID: 10546104
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Delineation of a recognisable phenotype of interstitial deletion 3 (q22.3q25.1) in a case with previously unreported truncus arteriosus.
    Rea G; McCullough S; McNerlan S; Craig B; Morrison PJ
    Eur J Med Genet; 2010; 53(3):162-7. PubMed ID: 20215058
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Further delineation of deletion 1p36 syndrome in 60 patients: a recognizable phenotype and common cause of developmental delay and mental retardation.
    Battaglia A; Hoyme HE; Dallapiccola B; Zackai E; Hudgins L; McDonald-McGinn D; Bahi-Buisson N; Romano C; Williams CA; Brailey LL; Zuberi SM; Carey JC
    Pediatrics; 2008 Feb; 121(2):404-10. PubMed ID: 18245432
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A small deletion of 16q23.1-->16q24.2 [del(16)(q23.1q24.2).ish del(16)(q23.1q24.2)(D16S395+, D16S348-, P5432+)] in a boy with iris coloboma and minor anomalies.
    Werner W; Kraft S; Callen DF; Bartsch O; Hinkel GK
    Am J Med Genet; 1997 Jun; 70(4):371-6. PubMed ID: 9182777
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Interstitial deletion of chromosome 2p15-16.1: report of two patients and critical review of current genotype-phenotype correlation.
    Piccione M; Piro E; Serraino F; Cavani S; Ciccone R; Malacarne M; Pierluigi M; Vitaloni M; Zuffardi O; Corsello G
    Eur J Med Genet; 2012 Apr; 55(4):238-44. PubMed ID: 22406401
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Diagnosis and fine mapping of a deletion in distal 11q in two Chinese patients with developmental delay.
    Ji T; Wu Y; Wang H; Wang J; Jiang Y
    J Hum Genet; 2010 Aug; 55(8):486-9. PubMed ID: 20520618
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 2q23.1 microdeletion of the MBD5 gene in a female with seizures, developmental delay and distinct dysmorphic features.
    Noh GJ; Graham JM
    Eur J Med Genet; 2012 May; 55(5):354-7. PubMed ID: 22659271
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Cryptic trisomy 5q35.2qter and deletion 1p36.3 characterised using FISH and array-based CGH.
    Utine EG; Alanay Y; Aktas D; Alikasifoglu M; Boduroglu K; Vermeesch J; Tuncbilek E; Fryns JP
    Eur J Med Genet; 2008; 51(4):343-50. PubMed ID: 18440888
    [TBL] [Abstract][Full Text] [Related]  

  • 18. De novo interstitial deletion in the long arm of chromosome 11: a case report.
    Li LL; Zhang HG; Shao XG; Gao JC; Zhang HY; Liu RZ
    Genet Mol Res; 2016 Jul; 15(2):. PubMed ID: 27421024
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Genotype-phenotype correlations in a new case of 8p23.1 deletion and review of the literature.
    Ballarati L; Cereda A; Caselli R; Selicorni A; Recalcati MP; Maitz S; Finelli P; Larizza L; Giardino D
    Eur J Med Genet; 2011; 54(1):55-9. PubMed ID: 20969981
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Polycystic kidneys and del (4)(q21.1q21.3): further delineation of a distinct phenotype.
    Velinov M; Kupferman J; Gu H; Macera MJ; Babu A; Jenkins EC; Kupchik G
    Eur J Med Genet; 2005; 48(1):51-5. PubMed ID: 15953406
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 15.