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 *

170 related articles for article (PubMed ID: 9677069)

  • 1. Interstitial deletion of the long arm of chromosome 4 [del(4)(q21.22q23)] and a liver tumor.
    Suwa K; Momoi MY; Yamagata T; Mori Y
    Am J Med Genet; 1998 Jul; 78(3):291-3. PubMed ID: 9677069
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Additional patient with del(12)(q21.2q22): further evidence for a candidate region for cardio-facio-cutaneous syndrome?
    Rauen KA; Albertson DG; Pinkel D; Cotter PD
    Am J Med Genet; 2002 Jun; 110(1):51-6. PubMed ID: 12116271
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Brief clinical report: interstitial deletion of the long arm of chromosome 4, del(4)(q28-->q31.3).
    Copelli S; del Rey G; Heinrich J; Coco R
    Am J Med Genet; 1995 Jan; 55(1):77-9. PubMed ID: 7702102
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Infantile hemangioendothelioma of the liver in patient with interstitial deletion of chromosome 6q: report of an autopsy case.
    Ito H; Yamasaki T; Okamoto O; Tahara E
    Am J Med Genet; 1989 Nov; 34(3):325-9. PubMed ID: 2596522
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Interstitial deletions 4q21.1q25 and 4q25q27: phenotypic variability and relation to Rieger anomaly.
    Kulharya AS; Maberry M; Kukolich MK; Day DW; Schneider NR; Wilson GN; Tonk V
    Am J Med Genet; 1995 Jan; 55(2):165-70. PubMed ID: 7717415
    [TBL] [Abstract][Full Text] [Related]  

  • 7. An 8-cM interstitial deletion on 4q21-q22 in DNA from an infant with hepatoblastoma overlaps with a commonly deleted region in adult liver cancers.
    Terada Y; Imoto I; Nagai H; Suwa K; Momoi M; Tajiri T; Onda M; Inazawa J; Emi M
    Am J Med Genet; 2001 Oct; 103(2):176-80. PubMed ID: 11568928
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Subtle overlapping deletions in the terminal region of chromosome 6q24.2-q26: three cases studied using FISH.
    Sukumar S; Wang S; Hoang K; Vanchiere CM; England K; Fick R; Pagon B; Reddy KS
    Am J Med Genet; 1999 Nov; 87(1):17-22. PubMed ID: 10528241
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Del(1)(q22-q25) syndrome. Cytogenetics and phenotype].
    Zaletaev DV; Dadali EL; Kuleshov NP
    Tsitol Genet; 1987; 21(3):213-6. PubMed ID: 3617217
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Terminal deletion of the long arm of chromosome 4. Report of a case of 46, XY, del(4)(q31) and review of 4q- syndrome.
    Yu CW; Chen H; Baucum RW; Hand AM
    Ann Genet; 1981; 24(3):158-61. PubMed ID: 6974525
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. A patient with an interstitial deletion of the proximal portion of the long arm of chromosome 4.
    Beall MH; Falk RE; Ying KL
    Am J Med Genet; 1988 Nov; 31(3):553-7. PubMed ID: 3067576
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Distal del(4) (q33) syndrome: detailed clinical presentation and molecular description with array-CGH.
    Kitsiou-Tzeli S; Sismani C; Koumbaris G; Ioannides M; Kanavakis E; Kolialexi A; Mavrou A; Touliatou V; Patsalis PC
    Eur J Med Genet; 2008; 51(1):61-7. PubMed ID: 17998173
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. 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]  

  • 17. Holoprosencephaly, ear abnormalities, congenital heart defect, and microphallus in a patient with 11q- mosaicism.
    Helmuth RA; Weaver DD; Wills ER
    Am J Med Genet; 1989 Feb; 32(2):178-81. PubMed ID: 2494886
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Proximal interstitial deletion of 7q: a case report and review of the literature.
    Zackowski JL; Raffel LJ; Blank CA; Schwartz S
    Am J Med Genet; 1990 Jul; 36(3):328-32. PubMed ID: 2194394
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Deletion 4q21/4q22 syndrome: two patients with de novo 4q21.3q23 and 4q13.2q23 deletions.
    Nowaczyk MJ; Teshima IE; Siegel-Bartelt J; Clarke JT
    Am J Med Genet; 1997 Apr; 69(4):400-5. PubMed ID: 9098490
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.