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 *

155 related articles for article (PubMed ID: 3901750)

  • 1. Deficiency of chromosome 8p21.1----8pter: case report and review of the literature.
    Dobyns WB; Dewald GW; Carlson RO; Mair DD; Michels VV
    Am J Med Genet; 1985 Sep; 22(1):125-34. PubMed ID: 3901750
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Interstitial deletion of the long arm of chromosome 2: case report and review of literature.
    Taysi K; Dengler DR; Jones LA; Heersma JR
    Ann Genet; 1981; 24(4):245-7. PubMed ID: 7036843
    [No Abstract]   [Full Text] [Related]  

  • 3. Phenotype associated with ring 10 chromosome: report of patient and review of literature.
    Michels VV; Driscoll DJ; Ledbetter DH; Riccardi VM
    Am J Med Genet; 1981; 9(3):231-7. PubMed ID: 7025632
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Deletion 11q23-->qter (Jacobsen syndrome). Report of three new patients.
    Obregon MG; Mingarelli R; Digilio MC; Zelante L; Giannotti A; Sabatino G; Dallapiccola B
    Ann Genet; 1992; 35(4):208-12. PubMed ID: 1296516
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Deletion of a portion of the long arm of chromosome 6.
    Goldberg R; Fish B; Ship A; Shprintzen RJ
    Am J Med Genet; 1980; 5(1):73-80. PubMed ID: 7395903
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Loss of the 3p25.3 band is critical in the manifestation of del(3p) syndrome: karyotype-phenotype correlation in cases with deficiency of the distal portion of the short arm of chromosome 3.
    Narahara K; Kikkawa K; Murakami M; Hiramoto K; Namba H; Tsuji K; Yokoyama Y; Kimoto H
    Am J Med Genet; 1990 Feb; 35(2):269-73. PubMed ID: 2178418
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Deletions of the long arm of chromosome 6: two new cases and review of the literature.
    Young RS; Fidone GS; Reider-Garcia PA; Hansen KL; McCombs JL; Moore CM
    Am J Med Genet; 1985 Jan; 20(1):21-9. PubMed ID: 3881954
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Partial duplication of distal 17q.
    Bridge J; Sanger W; Mosher G; Buehler B; Hearty C; Olney A; Fordyce R
    Am J Med Genet; 1985 Oct; 22(2):229-35. PubMed ID: 4050855
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Interstitial deletion of (17)(p11.2p11.2): report of six additional patients with a new chromosome deletion syndrome.
    Stratton RF; Dobyns WB; Greenberg F; DeSana JB; Moore C; Fidone G; Runge GH; Feldman P; Sekhon GS; Pauli RM
    Am J Med Genet; 1986 Jul; 24(3):421-32. PubMed ID: 3728561
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Deletion of the distal long arm of chromosome 1: a definable syndrome.
    Johnson VP; Heck LJ; Carter GA; Flom JO
    Am J Med Genet; 1985 Dec; 22(4):685-94. PubMed ID: 4073121
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Brief clinical report: two children with de novo del(9p).
    Young RS; Bader P; Palmer CG; Kaler SG; Hodes ME
    Am J Med Genet; 1983 Apr; 14(4):751-7. PubMed ID: 6846405
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Effect of the size of the deletion and clinical manifestation in Wolf-Hirschhorn syndrome: analysis of 13 patients with a de novo deletion.
    Wieczorek D; Krause M; Majewski F; Albrecht B; Horn D; Riess O; Gillessen-Kaesbach G
    Eur J Hum Genet; 2000 Jul; 8(7):519-26. PubMed ID: 10909852
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. The 8p- syndrome.
    Reiss JA; Brenes PM; Chamberlin J; Magenis RE; Lovrien EW
    Hum Genet; 1979 Mar; 47(2):135-40. PubMed ID: 437781
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Interstitial deletion of 8q21-->22 associated with minor anomalies, congenital heart defect, and Dandy-Walker variant.
    Donahue ML; Ryan RM
    Am J Med Genet; 1995 Mar; 56(1):97-100. PubMed ID: 7747796
    [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. Partial deletion of chromosome 6p: delineation of the syndrome.
    Palmer CG; Bader P; Slovak ML; Comings DE; Pettenati MJ
    Am J Med Genet; 1991 May; 39(2):155-60. PubMed ID: 2063917
    [TBL] [Abstract][Full Text] [Related]  

  • 18. De novo interstitial deletion of the long arm of chromosome 7:46,XY,del(7)(q23;q32).
    Martin-Pont B; Pilczer C; Dandine M; Tamboise A
    Ann Genet; 1985; 28(4):251-3. PubMed ID: 3879441
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 7q deletion syndrome (7q32 leads to 7qter).
    Harris EL; Wappner RS; Palmer CG; Hall B; Dinno N; Seashore MR; Breg WR
    Clin Genet; 1977 Oct; 12(4):233-8. PubMed ID: 912940
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Interstitial deletion 2q31 leads to q33.
    Buchanan PD; Rhodes RL; Stevenson CE
    Am J Med Genet; 1983 May; 15(1):121-6. PubMed ID: 6683075
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.