BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

138 related articles for article (PubMed ID: 10995503)

  • 1. Lung hypoplasia in a patient with del(2)(q33-q35) demonstrated by chromosome microdissection.
    Kramer BW; Martin T; Henn W; Lal S; Speer CP
    Am J Med Genet; 2000 Sep; 94(3):184-8. PubMed ID: 10995503
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Distal deletion, del(2)(q33.3q33.3), in a patient with severe growth deficiency and minor anomalies.
    Riegel M; Morava E; Czakó M; Kosztolányi G; Schinzel A
    Am J Med Genet; 2001 Aug; 102(3):227-30. PubMed ID: 11484198
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Interstitial deletion 2q33.3-q34 in a boy with a phenotype resembling the Seckel syndrome.
    Courtens W; Speleman F; Messiaen L; Bormans J; Van Roy N; Vamos E
    Am J Med Genet; 1997 Sep; 71(4):479-85. PubMed ID: 9286460
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Interstitial deletion of the distal long arm of chromosome 4, del (4)(q33-q35), in association with paternal balanced translocation.
    Mdzin R; Ko C; Abdul Latif Z; Zakaria Z
    Singapore Med J; 2008 Nov; 49(11):e336-9. PubMed ID: 19037546
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Cardio-facio-cutaneous syndrome phenotype in an individual with an interstitial deletion of 12q: identification of a candidate region for CFC syndrome.
    Rauen KA; Cotter PD; Bitts SM; Cox VA; Golabi M
    Am J Med Genet; 2000 Jul; 93(3):219-22. PubMed ID: 10925386
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Deletion of chromosome region 18q21.1 --> 18q21.3 in a patient without clinical features of the 18q- phenotype.
    Engelen JJ; Moog U; Weber J; Haagen AA; van Uum CM; Hamers AJ
    Am J Med Genet A; 2003 Jun; 119A(3):356-9. PubMed ID: 12784305
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Ocular anomalies associated with interstitial deletion of chromosome 2q31: case report and review.
    Gambrelle J; Till M; Lukusa B; Beby F; Mory N; Sann L; Kodjikian L; Grange JD; Putet G
    Ophthalmic Genet; 2007 Jun; 28(2):105-9. PubMed ID: 17558854
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Molecular cytogenetic characterization of a 2q35-q37 duplication and a 4q35.1-q35.2 deletion in two cousins: a genotype-phenotype analysis.
    Ronzoni L; Peron A; Bianchi V; Baccarin M; Guerneri S; Silipigni R; Lalatta F; Bedeschi MF
    Am J Med Genet A; 2015 Jul; 167(7):1551-9. PubMed ID: 25851921
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A review of phenotype-karyotype correlations in individuals with interstitial deletions of the long arm of chromosome 2.
    Ramer JC; Ladda RL; Frankel CA; Beckford A
    Am J Med Genet; 1989 Mar; 32(3):359-63. PubMed ID: 2658585
    [TBL] [Abstract][Full Text] [Related]  

  • 11. An unusual reciprocal translocation detected by subtelomeric FISH: interstitial and not terminal.
    Riegel M; Baumer A; Süss J; Schinzel A
    Am J Med Genet A; 2005 May; 135(1):86-90. PubMed ID: 15809996
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The 4q-Syndrome.
    Strehle EM; Ahmed OA; Hameed M; Russell A
    Genet Couns; 2001; 12(4):327-39. PubMed ID: 11837601
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Array based characterization of a terminal deletion involving chromosome subband 15q26.2: an emerging syndrome associated with growth retardation, cardiac defects and developmental delay.
    Davidsson J; Collin A; Björkhem G; Soller M
    BMC Med Genet; 2008 Jan; 9():2. PubMed ID: 18194513
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A case of ring chromosome 2 with growth retardation, mild dysmorphism, and microdeletion of 2p detected using FISH.
    Dee SL; Clark AT; Willatt LR; Yates JR
    J Med Genet; 2001 Sep; 38(9):E32. PubMed ID: 11546833
    [No Abstract]   [Full Text] [Related]  

  • 15. Terminal deletion of the long arm of chromosome 2 in a mildly dysmorphic hypotonic infant with karyotype 46,XY,del(2)(q37).
    Gorski JL; Cox BA; Kyine M; Uhlmann W; Glover TW
    Am J Med Genet; 1989 Mar; 32(3):350-2. PubMed ID: 2729355
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Pericentric inversion with partial 7(q35-->qter) duplication and 7pter deletion: diagnosis by cytogenetic and fish analysis in a 29-year-old male patient.
    Lukusa T; Van Buggenhout G; Devriendt K; Fryns JP
    Genet Couns; 2002; 13(1):1-10. PubMed ID: 12017231
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Multicolor chromosomal bar coding characterizes a de novo interstitial deletion (5)(q33.3q35.2) in a child with multiple congenital malformations.
    Schiffer C; Popp S; Moshir S; Rupprath G; Düngfelder E; Hager HD; Tariverdian G; Jauch A
    Clin Dysmorphol; 2003 Apr; 12(2):129-31. PubMed ID: 12868477
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Partial trisomy 2q: report of a patient with dup (2)(q33.1q35).
    Sebold CD; Romie S; Szymanska J; Torres-Martinez W; Thurston V; Muesing C; Vance GH
    Am J Med Genet A; 2005 Apr; 134A(1):80-3. PubMed ID: 15690398
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Trisomy 2q35-q37 due to insertion of 2q material into 17q25: clinical, cytogenetic, and molecular cytogenetic characterization.
    Fritz B; Müller-Navia J; Hillig U; Köhler M; Aslan M; Rehder H
    Am J Med Genet; 1999 Dec; 87(4):297-301. PubMed ID: 10588833
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A new case of an interstitial deletion (4)(q25q27) characterised by molecular cytogenetic techniques and review of the literature.
    Becker SA; Popp S; Rager K; Jauch A
    Eur J Pediatr; 2003 Apr; 162(4):267-70. PubMed ID: 12647202
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.