BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

146 related articles for article (PubMed ID: 6624439)

  • 1. De novo interstitial deletion of the long arm of chromosome 2 in a malformed newborn with a karyotype: 46,XY,del(2)(q12q14).
    Antich J; Carbonell X; Mas J; Clusellas N
    Acta Paediatr Scand; 1983 Jul; 72(4):631-3. PubMed ID: 6624439
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Interstitial deletion of the long arm of chromosome 2 in a polymalformed newborn--karyotype: 46,XX,del(2)(q21;q24).
    Fryns JP; Van Bosstraeten B; Malbrain H; Van den Berghe H
    Hum Genet; 1977 Nov; 39(2):233-8. PubMed ID: 598832
    [TBL] [Abstract][Full Text] [Related]  

  • 3. De novo interstitial deletion del(1)(p21p32).
    Bene M; Duca-Marinescu A; Ioan D; Maximilian C
    J Med Genet; 1979 Aug; 16(4):323-7. PubMed ID: 490590
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Interstitial deletion of the long arm of chromosome 1 [del(1)(q32q42)].
    Al-Awadi SA; Farag TI; Usha R; el-Khalifa MY; Sundareshan TS; Al-Othman SA
    Am J Med Genet; 1986 Apr; 23(4):931-3. PubMed ID: 3963055
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Interstitial deletion of the long arm of chromosome 3.
    Martsolf JT; Ray M
    Ann Genet; 1983; 26(2):98-9. PubMed ID: 6604494
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Interstitial deletion of chromosome 2 region in a malformed infant.
    Melnyk AR; Muraskas J
    Am J Med Genet; 1993 Jan; 45(1):49-51. PubMed ID: 8418659
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Newborn infant with inherited ring and de novo interstitial deletion on homologous chromosome 22s.
    Wenger SL; Boone LY; Cummins JH; Del Vecchio MA; Bay CA; Hummel M; Mowery-Rushton PA
    Am J Med Genet; 2000 Apr; 91(5):351-4. PubMed ID: 10766997
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Interstitial deletion of the long arm of chromosome 8. Karyotype: 46,XY,del(8)(q21).
    Fryns JP; Logghe N; Van Eygen M; Van Der Berghe H
    Hum Genet; 1979 Apr; 48(1):127-30. PubMed ID: 457127
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A girl with an interstitial deletion of the short arm of chromosome 3 studied with a high-resolution banding technique.
    Sichong Z; Bui TH; Castro I; Iselius L; Håkansson S; Lundmark KM
    Hum Genet; 1981; 59(2):178-81. PubMed ID: 7327578
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Prenatal diagnosis of de novo mosaic deletion 13q associated with multiple abnormalities.
    Widschwendter A; Riha K; Duba HC; Kreczy A; Marth C; Schwärzler P
    Ultrasound Obstet Gynecol; 2002 Apr; 19(4):396-9. PubMed ID: 11952971
    [TBL] [Abstract][Full Text] [Related]  

  • 11. De novo interstitial deletion of 1p (pter----p34.1::p32.3----qter).
    Yoshino M; Watanabe Y; Harada N; Abe K
    J Med Genet; 1991 Aug; 28(8):539-40. PubMed ID: 1920371
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Terminal deletion of the long arm of chromosome 2 in a premature infant with karyotype: 46,XY,del(2)(q37).
    Wang TH; Johnston K; Hsieh CL; Dennery PA
    Am J Med Genet; 1994 Feb; 49(4):399-401. PubMed ID: 8160733
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Centric fission of chromosome 7 with 47,XX,del(7)(pter----cen::q21----qter)+cen fr karyotype in a mother and proximal 7q deletion in two malformed newborns.
    Fryns JP; Kleczkowska A; Limbos C; Vandecasseye W; Van den Berghe H
    Ann Genet; 1985; 28(4):248-50. PubMed ID: 3879440
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A child with multiple congenital anomalies and karyotype 46,XY,del(14)(q31q32.3): further delineation of chromosome 14 interstitial deletion syndrome.
    Gorski JL; Uhlmann WR; Glover TW
    Am J Med Genet; 1990 Dec; 37(4):471-4. PubMed ID: 2260590
    [TBL] [Abstract][Full Text] [Related]  

  • 15. De novo interstitial deletion of chromosome 1p with absent corpus callosum--a case report.
    Sivasankaran S; Ho NK; Knight L
    Ann Acad Med Singap; 1997 Jul; 26(4):507-9. PubMed ID: 9395821
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Severe clinical phenotype due to an interstitial deletion of the short arm of chromosome 1: a brief review.
    Stockton DW; Ross HL; Bacino CA; Altman CA; Shaffer LG; Lupski JR
    Am J Med Genet; 1997 Aug; 71(2):189-93. PubMed ID: 9217220
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A second patient with partial deletion of the short arm of chromosome 3: karyotype 46,XY,del(3)(p25).
    Higginbottom MC; Mascarello JT; Hassin H; McCord WK
    J Med Genet; 1982 Feb; 19(1):71-3. PubMed ID: 7069751
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Multiple congenital anomalies/mental retardation (MCA/MR) syndrome due to interstitial deletion 1q.
    Steinbach P; Wolf M; Schmidt H
    Am J Med Genet; 1984 Sep; 19(1):131-6. PubMed ID: 6496565
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Deletion of the short arm of chromosome 3: a case report with necropsy findings.
    Beneck D; Suhrland MJ; Dicker R; Greco MA; Wolman SR
    J Med Genet; 1984 Aug; 21(4):307-10. PubMed ID: 6492097
    [TBL] [Abstract][Full Text] [Related]  

  • 20. De novo del(3)(q2800).
    Alvarez Arratia MC; Rivera H; Möller M; Valdivia A; Vigueras A; Cantu JM
    Ann Genet; 1984; 27(2):109-11. PubMed ID: 6331786
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.