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 *

136 related articles for article (PubMed ID: 305761)

  • 1. Deletion of the long arm of chromosome 4 [46,XX,del(4)(q31)] in a patient with congenital anomalies.
    Back E; Hertel C; Vogel W; Bettecken F; Thiesen M
    Ann Genet; 1977 Dec; 20(4):294-6. PubMed ID: 305761
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Brief cytogenetic case report: a 4.5-year-old girl with deletion 4q syndrome--de novo, 46,XX, del(4) (pter leads to q31:).
    Young RS; Palmer CG; Bender HA; Weaver DD; Hodes ME
    Am J Med Genet; 1982 May; 12(1):103-7. PubMed ID: 7091193
    [No Abstract]   [Full Text] [Related]  

  • 3. Deletion 2q37: an identifiable clinical syndrome with mental retardation and autism.
    Galasso C; Lo-Castro A; Lalli C; Nardone AM; Gullotta F; Curatolo P
    J Child Neurol; 2008 Jul; 23(7):802-6. PubMed ID: 18658079
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Partial deletion of the long arm of chromosome 13 (q32q33.2) associated with mental retardation, choanal atresia and fish mouth.
    Balci S; Yuksel Konuk B; Atik F; Oguz AK; Ergun MA; Baltaci V; Kosyakova N; Liehr T
    Genet Couns; 2010; 21(3):317-24. PubMed ID: 20964123
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Unusual chromosomal mosaicism in Wolf-Hirschhorn syndrome: del(4)(p16)/der(4)(qter-q31.3::pter-qter).
    Syrrou M; Borghgraef M; Fryns JP
    Am J Med Genet; 2001 Dec; 104(3):199-203. PubMed ID: 11754044
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Terminal deletion 4q in a severely retarded boy.
    de Michelena MI; Campos PJ
    Am J Med Genet; 1989 Jun; 33(2):228-30. PubMed ID: 2764033
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Phenotypic variability of del(2) (q22-q23): report of a case with a review of the literature.
    Lurie IW; Supovitz KR; Rosenblum-Vos LS; Wulfsberg EA
    Genet Couns; 1994; 5(1):11-4. PubMed ID: 8031530
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. 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]  

  • 12. A case of partial 9p monosomy with some unusual clinical features.
    Rutten FJ; Hustinx TW; Dunk-Tillemans AA; Scheres JM; Tjon YS
    Ann Genet; 1978 Mar; 21(1):51-5. PubMed ID: 308344
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Syndromes associated with deletion of the long arm of chromosome 18[del(18q)].
    Wilson MG; Towner JW; Forsman I; Siris E
    Am J Med Genet; 1979; 3(2):155-74. PubMed ID: 474629
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. 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]  

  • 16. Two patients with chromosome 6q terminal deletions with breakpoints at q24.3 and q25.3.
    Meng J; Fujita H; Nagahara N; Kashiwai A; Yoshioka Y; Funato M
    Am J Med Genet; 1992 Jul; 43(4):747-50. PubMed ID: 1621768
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. 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]  

  • 19. Syndrome of proximal interstitial deletion 4p15: report of three cases and review of the literature.
    Chitayat D; Ruvalcaba RH; Babul R; Teshima IE; Posnick JC; Vekemans MJ; Scarpelli H; Thuline H
    Am J Med Genet; 1995 Jan; 55(2):147-54. PubMed ID: 7717413
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Interstitial del(13q) associated with blindness and mental retardation.
    Juberg RC; Mowrey PN
    Am J Med Genet; 1984 Mar; 17(3):609-13. PubMed ID: 6711612
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.