BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

122 related articles for article (PubMed ID: 7516119)

  • 1. Deletion (11)(q14.1q21).
    Stratton RF; Lazarus KH; Ritchie EJ; Bell AM
    Am J Med Genet; 1994 Feb; 49(3):294-8. PubMed ID: 7516119
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Interstitial deletion of 8q13.3-->22.1 associated with craniosynostosis.
    Fryburg JS; Golden WL
    Am J Med Genet; 1993 Mar; 45(5):638-41. PubMed ID: 7681252
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Interstitial deletion of the long arm of chromosome 11: report of a case and review of the literature.
    Wakazono A; Masuno M; Yamaguchi S; Tsubouchi K; Kondo N; Orii T
    Jpn J Hum Genet; 1992 Sep; 37(3):229-34. PubMed ID: 1472705
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Deletion (14) (q24.3q32.1): evidence for a distinct clinical phenotype.
    Karnitis SA; Burns K; Sudduth KW; Golden WL; Wilson WG
    Am J Med Genet; 1992 Sep; 44(2):153-7. PubMed ID: 1280909
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Interstitial deletion of chromosome 18[del(18)(q11.2q12.2 or q12.2q21.1].
    Surh LC; Ledbetter DH; Greenberg F
    Am J Med Genet; 1991 Oct; 41(1):15-7. PubMed ID: 1719812
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Interstitial deletion of 11q.
    Guć-Sćekić M; Pilić-Radivojević G; Mrdjenović G; Djurić M
    J Med Genet; 1989 Mar; 26(3):205-6. PubMed ID: 2468775
    [No Abstract]   [Full Text] [Related]  

  • 9. Tetrasomy 15q25.3 --> qter resulting from an analphoid supernumerary marker chromosome in a patient with multiple anomalies and bilateral Wilms tumors.
    Hu J; McPherson E; Surti U; Hasegawa SL; Gunawardena S; Gollin SM
    Am J Med Genet; 2002 Nov; 113(1):82-8. PubMed ID: 12400070
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. M-banding characterization of a 16p11.2p13.1 tandem duplication in a child with autism, neurodevelopmental delay and dysmorphism.
    Behjati F; Shafaghati Y; Firouzabadi SG; Kahrizi K; Bagherizadeh I; Najmabadi H; Bint S; Ogilvie C
    Eur J Med Genet; 2008; 51(6):608-14. PubMed ID: 18674645
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Partial trisomy of chromosome 6q: an interstitial duplication of the long arm.
    Zneimer SM; Ziel B; Bachman R
    Am J Med Genet; 1998 Nov; 80(2):133-5. PubMed ID: 9805129
    [TBL] [Abstract][Full Text] [Related]  

  • 13. De novo 10q22 interstitial deletion.
    Cook L; Weaver DD; Hartsfield JK; Vance GH
    J Med Genet; 1999 Jan; 36(1):71-2. PubMed ID: 9950372
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Interstitial deletion of the short arm of chromosome 8: report of a patient and review of the literature.
    Plomp AS; Schrander-Stumpel CT; Engelen JJ; Sijstermans JM; Loneus WH; Fryns JP
    Genet Couns; 1995; 6(1):55-60. PubMed ID: 7794563
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Microcephaly/lymphedema and terminal deletion of the long arm of chromosome 13.
    Fryns JP
    Am J Med Genet; 1995 Jul; 57(3):504. PubMed ID: 7545871
    [No Abstract]   [Full Text] [Related]  

  • 16. Loss of heterozygosity for the short arm of chromosome 7 in sporadic Wilms tumour.
    Grundy RG; Pritchard J; Scambler P; Cowell JK
    Oncogene; 1998 Jul; 17(3):395-400. PubMed ID: 9690521
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Interstitial deletion of chromosome 10, del(10) (q11.2q22.1) in a boy with developmental delay and multiple congenital anomalies.
    Zenger-Hain JL; Roberson J; Van Dyke DL; Weiss L
    Am J Med Genet; 1993 Jun; 46(4):438-40. PubMed ID: 7689299
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Molecular-cytogenetic identification of partial trisomy of a short arm of chromosome 8].
    Zerova-Liubimova TE; Rigel M; Smul'skaia NA; Evseenkova EG; Gorovenko NG; Shintzel A
    Tsitol Genet; 2004; 38(4):55-61. PubMed ID: 15715166
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Terminal deletion of the long arm of chromosome 10: a new case with breakpoint in q25.3.
    Petersen B; Strassburg HM; Feichtinger W; Kress W; Schmid M
    Am J Med Genet; 1998 Apr; 77(1):60-2. PubMed ID: 9557896
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.