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 *

118 related articles for article (PubMed ID: 17394389)

  • 1. A girl with del(4)(q33) and occipital encephalocele: clinical description and molecular genetic characterization of a rare patient.
    Quadrelli R; Strehle EM; Vaglio A; Larrandaburu M; Mechoso B; Quadrelli A; Fan YS; Huang T
    Genet Test; 2007; 11(1):4-10. PubMed ID: 17394389
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Robin sequence and a deficiency of the left forearm in a girl with a deletion of chromosome 4q33-qter.
    Menko FH; Madan K; Baart JA; Beukenhorst HL
    Am J Med Genet; 1992 Nov; 44(5):696-8. PubMed ID: 1344067
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. The spectrum of 4q- syndrome illustrated by a case series.
    Strehle EM; Gruszfeld D; Schenk D; Mehta SG; Simonic I; Huang T
    Gene; 2012 Sep; 506(2):387-91. PubMed ID: 22771923
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Interstitial deletion 4q32-34 with ulnar deficiency: 4q33 may be the critical region in 4q terminal deletion syndrome.
    Keeling SL; Lee-Jones L; Thompson P
    Am J Med Genet; 2001 Mar; 99(2):94-8. PubMed ID: 11241465
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Terminal deletion of long arm of chromosome 4: patient report and literature review.
    Evers LJ; Schrander-Stumpel CT; Engelen JJ; Mulder H; Borghgraef M; Fryns JP
    Genet Couns; 1993; 4(2):139-45. PubMed ID: 7689326
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Interstitial deletion of the distal long arm of chromosome 4, del (4)(q33-q35), in association with paternal balanced translocation.
    Mdzin R; Ko C; Abdul Latif Z; Zakaria Z
    Singapore Med J; 2008 Nov; 49(11):e336-9. PubMed ID: 19037546
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Intercalary de novo deletion of chromosome 1: del(1) (q24 to q32)].
    Faugeras C; Barthe D
    J Genet Hum; 1985 Jan; 33(1):51-6. PubMed ID: 3981142
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Cytogenetic and molecular characterization of partial trisomy 4q and partial monosomy 10q in a patient].
    Zhang YL; Dai Y; Tu ZG; Li QY; Wang LQ; Zhang L; Zeng J; Ouyang ZB
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2010 Apr; 27(2):153-7. PubMed ID: 20376795
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A de novo proximal 6q deletion confirmed by array comparative genomic hybridization.
    Woo KS; Kim JE; Kim KE; Kim MJ; Yoo JH; Ahn HS; Shaffer LG; Han JY
    Korean J Lab Med; 2010 Feb; 30(1):84-8. PubMed ID: 20197728
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 5.78 Mb terminal deletion of chromosome 15q in a girl, evaluation of NR2F2 as candidate gene for congenital heart defects.
    Nakamura E; Makita Y; Okamoto T; Nagaya K; Hayashi T; Sugimoto M; Manabe H; Taketazu G; Kajino H; Fujieda K
    Eur J Med Genet; 2011; 54(3):354-6. PubMed ID: 21172461
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Inv dup del(10q): identification by fluorescence in situ hybridization and array comparative genomic hybridization in a fetus with two concurrent chromosomal rearrangements.
    Chen CP; Chen M; Su YN; Huang JP; Ma GC; Chang SP; Chern SR; Chen YT; Su JW; Lee CC; Town DD; Wang W
    Taiwan J Obstet Gynecol; 2012 Jun; 51(2):245-52. PubMed ID: 22795102
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Del(4)(q33----qter): another case report of a child with mild dysmorphism.
    Fagan KA; Morris RB
    J Med Genet; 1989 Dec; 26(12):776-8. PubMed ID: 2614797
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Further phenotypic delineation of subtelomeric (terminal) 4q deletion with emphasis on intracranial and reproductive anatomy.
    Sills ES; Burns MJ; Parker LD; Carroll LP; Kephart LL; Dyer CS; Papenhausen PR; Davis JG
    Orphanet J Rare Dis; 2007 Feb; 2():9. PubMed ID: 17295911
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Prenatal diagnosis of partial monosomy 13q associated with occipital encephalocoele in a fetus.
    Chen CP; Liu FF; Jan SW; Wang KG; Lan CC
    Prenat Diagn; 1996 Jul; 16(7):664-6. PubMed ID: 8843478
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Molecular cytogenetic characterization of the first reported case of an inv dup (4p)(p15.1-pter) with a concomitant 4q35.1-qter deletion and normal parents.
    Tassano E; Alpigiani MG; Salvati P; Gimelli S; Lorini R; Gimelli G
    Gene; 2012 Dec; 511(2):338-40. PubMed ID: 23031810
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Array based characterization of a terminal deletion involving chromosome subband 15q26.2: an emerging syndrome associated with growth retardation, cardiac defects and developmental delay.
    Davidsson J; Collin A; Björkhem G; Soller M
    BMC Med Genet; 2008 Jan; 9():2. PubMed ID: 18194513
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Schizencephaly accompanied by occipital encephalocele and deletion of chromosome 22q13.32: a case report.
    Inan C; Sayin NC; Gurkan H; Atli E; Gursoy Erzincan S; Uzun I; Sutcu H; Dogan S; Ikbal Atli E; Varol F
    Fetal Pediatr Pathol; 2019 Dec; 38(6):496-502. PubMed ID: 31130048
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.