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 *

152 related articles for article (PubMed ID: 17318845)

  • 1. Diagnosis of genetic abnormalities in developmentally delayed patients: a new strategy combining MLPA and array-CGH.
    Kriek M; Knijnenburg J; White SJ; Rosenberg C; den Dunnen JT; van Ommen GJ; Tanke HJ; Breuning MH; Szuhai K
    Am J Med Genet A; 2007 Mar; 143A(6):610-4. PubMed ID: 17318845
    [No Abstract]   [Full Text] [Related]  

  • 2. Use of targeted array-based CGH for the clinical diagnosis of chromosomal imbalance: is less more?
    Bejjani BA; Saleki R; Ballif BC; Rorem EA; Sundin K; Theisen A; Kashork CD; Shaffer LG
    Am J Med Genet A; 2005 Apr; 134(3):259-67. PubMed ID: 15723295
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Diagnosis of cryptic chromosome aberrations].
    Ness GO; Houge G
    Tidsskr Nor Laegeforen; 2003 Sep; 123(17):2418-21. PubMed ID: 14562774
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Prenatally diagnosed de novo segmental amplification or deletion by microarray-based comparative genomic hybridization: A retrospective study.
    Peng HH; Lee CH; Su SY; Chen KJ; Lee YC; You SH; Lee WF; Cheng PJ
    Taiwan J Obstet Gynecol; 2019 Sep; 58(5):662-666. PubMed ID: 31542089
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Development and validation of a CGH microarray for clinical cytogenetic diagnosis.
    Cheung SW; Shaw CA; Yu W; Li J; Ou Z; Patel A; Yatsenko SA; Cooper ML; Furman P; Stankiewicz P; Lupski JR; Chinault AC; Beaudet AL
    Genet Med; 2005; 7(6):422-32. PubMed ID: 16024975
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Development of a comparative genomic hybridization microarray and demonstration of its utility with 25 well-characterized 1p36 deletions.
    Yu W; Ballif BC; Kashork CD; Heilstedt HA; Howard LA; Cai WW; White LD; Liu W; Beaudet AL; Bejjani BA; Shaw CA; Shaffer LG
    Hum Mol Genet; 2003 Sep; 12(17):2145-52. PubMed ID: 12915473
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Transmitted duplication of 12q21.32-12q22 includes 48 genes and has no apparent phenotypic consequences.
    Barber JC; Maloney VK; Kirchhoff M; Thomas NS; Boyle TA; Castle B
    Am J Med Genet A; 2007 Mar; 143A(6):615-8. PubMed ID: 17318843
    [No Abstract]   [Full Text] [Related]  

  • 8. Development of new postnatal diagnostic methods for chromosome disorders.
    Shaffer LG; Bejjani BA
    Semin Fetal Neonatal Med; 2011 Apr; 16(2):114-8. PubMed ID: 21112262
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Comparative genomic hybridization by microarray for the detection of cytogenetic imbalance.
    Jarmuz M; Ballif BC; Kashork CD; Theisen AP; Bejjani BA; Shaffer LG
    Methods Mol Med; 2006; 128():23-31. PubMed ID: 17071987
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Special report: aCGH for the genetic evaluation of patients with developmental delay/mental retardation or autism spectrum disorder.
    Technol Eval Cent Assess Program Exec Summ; 2009 Apr; 23(10):1-5. PubMed ID: 19824216
    [No Abstract]   [Full Text] [Related]  

  • 11. 22q13 deletion syndrome: an update and review for the primary pediatrician.
    Havens JM; Visootsak J; Phelan MC; Graham JM
    Clin Pediatr (Phila); 2004; 43(1):43-53. PubMed ID: 14968892
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Array-CGH increased the diagnostic rate of developmental delay or intellectual disability in Taiwan.
    Lee CL; Lee CH; Chuang CK; Chiu HC; Chen YJ; Chou CL; Wu PS; Chen CP; Lin HY; Lin SP
    Pediatr Neonatol; 2019 Aug; 60(4):453-460. PubMed ID: 30581099
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Usefulness of high-resolution comparative genomic hybridization (CGH) for detecting and characterizing constitutional chromosome abnormalities.
    Ness GO; Lybaek H; Houge G
    Am J Med Genet; 2002 Nov; 113(2):125-36. PubMed ID: 12407702
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Identification of the origin of marker chromosome by comparative genomic hybridization].
    Zhou L; Wu LQ; Liang DS; Pan Q; Long ZG; Dai HP; Li J; Cai F; Xia K; Xia JH
    Zhong Nan Da Xue Xue Bao Yi Xue Ban; 2007 Apr; 32(2):264-7. PubMed ID: 17478934
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Pallister-Killian syndrome: Review of fetal phenotype.
    Thakur S; Gupta R; Tiwari B; Singh N; Saxena KK
    Clin Genet; 2019 Jan; 95(1):79-84. PubMed ID: 29790157
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Strategies to identify supernumerary chromosomal markers in constitutional cytogenetics].
    Douet-Guilbert N; Basinko A; Le Bris MJ; Herry A; Morel F; De Braekeleer M
    Pathol Biol (Paris); 2008 Sep; 56(6):362-7. PubMed ID: 18456432
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Gene dosage methods as diagnostic tools for the identification of chromosome abnormalities.
    Gouas L; Goumy C; Véronèse L; Tchirkov A; Vago P
    Pathol Biol (Paris); 2008 Sep; 56(6):345-53. PubMed ID: 18513889
    [TBL] [Abstract][Full Text] [Related]  

  • 18. No detectable genomic aberrations by BAC array CGH in Kabuki make-up syndrome patients.
    Miyake N; Shimokawa O; Harada N; Sosonkina N; Okubo A; Kawara H; Okamoto N; Ohashi H; Kurosawa K; Naritomi K; Kaname T; Nagai T; Shotelersuk V; Hou JW; Fukushima Y; Kondoh T; Matsumoto T; Shinoki T; Kato M; Tonoki H; Nomura M; Yoshiura K; Kishino T; Ohta T; Niikawa N; Matsumoto N
    Am J Med Genet A; 2006 Feb; 140(3):291-3. PubMed ID: 16278908
    [No Abstract]   [Full Text] [Related]  

  • 19. A novel interstitial microdeletion of 7q22.1-7q22.3 detected by array comparative genomic hybridization.
    Al-Hassnan ZN; Al-Bakheet A; Abu-Dheim N; Al-Younes B; Colak D; Kaya N
    Am J Med Genet A; 2011 Dec; 155A(12):3128-31. PubMed ID: 22002944
    [No Abstract]   [Full Text] [Related]  

  • 20. A 137-kb deletion within the Potocki-Shaffer syndrome interval on chromosome 11p11.2 associated with developmental delay and hypotonia.
    Montgomery ND; Turcott CM; Tepperberg JH; McDonald MT; Aylsworth AS
    Am J Med Genet A; 2013 Jan; 161A(1):198-202. PubMed ID: 23239541
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.