BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

392 related articles for article (PubMed ID: 3067575)

  • 1. Interstitial and terminal deletions of the long arm of chromosome 4: further delineation of phenotypes.
    Lin AE; Garver KL; Diggans G; Clemens M; Wenger SL; Steele MW; Jones MC; Israel J
    Am J Med Genet; 1988 Nov; 31(3):533-48. PubMed ID: 3067575
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Deletions of different segments of the long arm of chromosome 4.
    Mitchell JA; Packman S; Loughman WD; Fineman RM; Zackai E; Patil SR; Emanual B; Bartley JA; Hanson JW
    Am J Med Genet; 1981; 8(1):73-89. PubMed ID: 7246608
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Interstitial deletions of the short arm of chromosome 4 in patients with a similar combination of multiple minor anomalies and mental retardation.
    White DM; Pillers DA; Reiss JA; Brown MG; Magenis RE
    Am J Med Genet; 1995 Jul; 57(4):588-97. PubMed ID: 7573135
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 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]  

  • 6. Terminal and interstitial deletions of the long arm of chromosome 7: a review with five new cases.
    Young RS; Weaver DD; Kukolich MK; Heerema NA; Palmer CG; Kawira EL; Bender HA
    Am J Med Genet; 1984 Feb; 17(2):437-50. PubMed ID: 6199974
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. 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]  

  • 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. Interstitial deletion of long arm of chromosome 13.
    Carnevale A; Frias S; Alcantar R
    Ann Genet; 1984; 27(1):49-52. PubMed ID: 6609673
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Terminal deletion of chromosome 10q26: delineation of two clinical phenotypes.
    Petit P; Devriendt K; Azou M; Gewillig M; Fryns JP
    Genet Couns; 1998; 9(4):271-5. PubMed ID: 9894164
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Further delineation of deletion 1p36 syndrome in 60 patients: a recognizable phenotype and common cause of developmental delay and mental retardation.
    Battaglia A; Hoyme HE; Dallapiccola B; Zackai E; Hudgins L; McDonald-McGinn D; Bahi-Buisson N; Romano C; Williams CA; Brailey LL; Zuberi SM; Carey JC
    Pediatrics; 2008 Feb; 121(2):404-10. PubMed ID: 18245432
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Interstitial deletion of (17)(p11.2p11.2) in nine patients.
    Smith AC; McGavran L; Robinson J; Waldstein G; Macfarlane J; Zonona J; Reiss J; Lahr M; Allen L; Magenis E
    Am J Med Genet; 1986 Jul; 24(3):393-414. PubMed ID: 2425619
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Child with velocardiofacial syndrome and del (4)(q34.2): another critical region associated with a velocardiofacial syndrome-like phenotype.
    Tsai CH; Van Dyke DL; Feldman GL
    Am J Med Genet; 1999 Feb; 82(4):336-9. PubMed ID: 10051168
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A specific syndrome due to deletion of the distal long arm of chromosome 1.
    Meinecke P; Vögtel D
    Am J Med Genet; 1987 Oct; 28(2):371-6. PubMed ID: 3322005
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. 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]  

  • 18. 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]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 20.