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 *

179 related articles for article (PubMed ID: 26773965)

  • 21. An adult patient with a distal interstitial 14q deletion: clinical report and literature review.
    Spruijt L; Van Der Blij-Philipsen M; Engelen JJ; Schrander-Stumpel CT
    Genet Couns; 2000; 11(4):335-40. PubMed ID: 11140410
    [TBL] [Abstract][Full Text] [Related]  

  • 22. A child with an inherited 0.31 Mb microdeletion of chromosome 14q32.33: further delineation of a critical region for the 14q32 deletion syndrome.
    Holder JL; Lotze TE; Bacino C; Cheung SW
    Am J Med Genet A; 2012 Aug; 158A(8):1962-6. PubMed ID: 22488736
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Terminal 14q deletion with unbalanced t(Y;14)(q12;q32) translocation.
    Bağcı G; Çetin GO; Semerci N; Toruner GA; Cinbiş M
    Clin Dysmorphol; 2012 Jan; 21(1):37-41. PubMed ID: 22143350
    [TBL] [Abstract][Full Text] [Related]  

  • 24. A case of 22q11.2 deletion syndrome with right microphthalmia and left corneal staphyloma.
    Tarlan B; Kiratli H; Kılıç E; Utine E; Boduroğlu K
    Ophthalmic Genet; 2014 Dec; 35(4):248-51. PubMed ID: 23834556
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Ocular colobomata.
    Onwochei BC; Simon JW; Bateman JB; Couture KC; Mir E
    Surv Ophthalmol; 2000; 45(3):175-94. PubMed ID: 11094243
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Microphthalmia, anophthalmia, and coloboma and associated ocular and systemic features: understanding the spectrum.
    Skalicky SE; White AJ; Grigg JR; Martin F; Smith J; Jones M; Donaldson C; Smith JE; Flaherty M; Jamieson RV
    JAMA Ophthalmol; 2013 Dec; 131(12):1517-24. PubMed ID: 24177921
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Real-world clinical and molecular management of 50 prospective patients with microphthalmia, anophthalmia and/or ocular coloboma.
    Harding P; Gore S; Malka S; Rajkumar J; Oluonye N; Moosajee M
    Br J Ophthalmol; 2023 Nov; 107(12):1925-1935. PubMed ID: 36192130
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Ring chromosome formation as a novel escape mechanism in patients with inverted duplication and terminal deletion.
    Knijnenburg J; van Haeringen A; Hansson KB; Lankester A; Smit MJ; Belfroid RD; Bakker E; Rosenberg C; Tanke HJ; Szuhai K
    Eur J Hum Genet; 2007 May; 15(5):548-55. PubMed ID: 17342151
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Biological and clinical characterization of recurrent 14q deletions in CLL and other mature B-cell neoplasms.
    Reindl L; Bacher U; Dicker F; Alpermann T; Kern W; Schnittger S; Haferlach T; Haferlach C
    Br J Haematol; 2010 Oct; 151(1):25-36. PubMed ID: 20649559
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Chromosome 6p25 deletion syndrome: report of a case with optic disc coloboma and review of published ophthalmic findings.
    Beby F; Des Portes V; Till M; Mottolese C; Denis P
    Ophthalmic Genet; 2012 Dec; 33(4):240-8. PubMed ID: 22497499
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Goyal-Naqvi Syndrome (Concurrent Trisomy 10p and Terminal 14q Deletion): A Review of the Literature.
    Goyal C; Goyal V; Naqvi WM
    Cureus; 2021 Jul; 13(7):e16652. PubMed ID: 34513343
    [TBL] [Abstract][Full Text] [Related]  

  • 32. FISH-mapping of telomeric 14q32 deletions: search for the cause of seizures.
    Schlade-Bartusiak K; Costa T; Summers AM; Nowaczyk MJ; Cox DW
    Am J Med Genet A; 2005 Oct; 138A(3):218-24. PubMed ID: 16152642
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Ocular manifestations of chromosome 14 terminal deletion.
    Chung I; Chawla R; FitzGerald DE
    J Pediatr Ophthalmol Strabismus; 2006; 43(2):104-6. PubMed ID: 16598978
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Bilateral retinoblastoma, microphthalmia, and colobomas in the 13q deletion syndrome.
    Schocket LS; Beaverson KL; Rollins IS; Abramson DH
    Arch Ophthalmol; 2003 Jun; 121(6):916-7. PubMed ID: 12796275
    [No Abstract]   [Full Text] [Related]  

  • 35. Colobomatous microphthalmia with midfacial clefting: part of the spectrum of branchio-oculo-facial syndrome?
    Richardson E; Davison C; Moore AT
    Ophthalmic Genet; 1996 Jun; 17(2):59-65. PubMed ID: 8832722
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Array comparative genomic hybridization analysis in patients with anophthalmia, microphthalmia, and coloboma.
    Raca G; Jackson CA; Kucinskas L; Warman B; Shieh JT; Schneider A; Bardakjian TM; Schimmenti LA
    Genet Med; 2011 May; 13(5):437-42. PubMed ID: 21285886
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 14q terminal deletion: prenatal diagnosis in a child with severe congenital anomalies.
    Mertens DJ; De Die-Smulders CE; Kampschöer PH; Offermans JP; Engelen JJ; Hamers AJ; Lammens M; Schrander-Stumpel CT
    Genet Couns; 2000; 11(4):341-6. PubMed ID: 11140411
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Delineation of 14q32.3 deletion syndrome.
    Ortigas AP; Stein CK; Thomson LL; Hoo JJ
    J Med Genet; 1997 Jun; 34(6):515-7. PubMed ID: 9192277
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Molecular and clinical characterization of patients with a ring chromosome 11.
    Hansson KB; Gijsbers AC; Oostdijk W; Rehbock JJ; de Snoo F; Ruivenkamp CA; Kant SG
    Eur J Med Genet; 2012 Dec; 55(12):708-14. PubMed ID: 22975011
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Whole Exome Sequencing in Coloboma/Microphthalmia: Identification of Novel and Recurrent Variants in Seven Genes.
    Haug P; Koller S; Maggi J; Lang E; Feil S; Wlodarczyk A; Bähr L; Steindl K; Rohrbach M; Gerth-Kahlert C; Berger W
    Genes (Basel); 2021 Jan; 12(1):. PubMed ID: 33418956
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.