BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

178 related articles for article (PubMed ID: 11755103)

  • 1. 18p deletion syndrome with a 45, XY, t (14; 18) (p11;q11.2), -18, karyotype.
    Rao VB; Kerketta L; Korgaonkar S; Ghosh K; Mohanty D
    Ann Genet; 2001; 44(4):187-90. PubMed ID: 11755103
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Further clinical delineation in trisomy 1q32 syndrome.
    Nuño-Arana I; González-García JR; García-Cruz D
    Ann Genet; 2001; 44(4):175-7. PubMed ID: 11755100
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Partial deletion of 18p and partial duplication of 18q caused by a paternal pericentric inversion.
    Israëls T; Hoovers J; Turpijn HM; Wijburg FA; Hennekam RC
    Clin Genet; 1996 Dec; 50(6):520-4. PubMed ID: 9147887
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Atypical 18p- syndrome associated with partial trisomy 16p in a chromosomally unbalanced child of consanguineous parents with an identical balanced translocation.
    Kupchik GS; Barrett SK; Babu A; Charria-Ortiz G; Velinov M; Macera MJ
    Eur J Med Genet; 2005; 48(1):57-65. PubMed ID: 15953407
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Basilar artery dolichoectasia in a boy with a combination of partial monosomy 18p and partial trisomy 20q.
    Su PH; Chen JY; Chen SJ; Yang MS; Liu YL
    Clin Dysmorphol; 2006 Oct; 15(4):225-228. PubMed ID: 16957478
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Ring chromosome 9 in a girl with developmental delay and dysmorphic features: case report and review of the literature.
    la Cour Sibbesen E; Jespersgaard C; Alosi D; Bisgaard AM; Tümer Z
    Am J Med Genet A; 2013 Jun; 161A(6):1447-52. PubMed ID: 23633410
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A 13-year-old girl with 18p deletion syndrome presenting Turner syndrome-like clinical features of short stature, short webbed neck, low posterior hair line, puffy eyelids and increased carrying angle of the elbows.
    Chen CP; Lin SP; Chern SR; Wu PS; Chen SW; Lai ST; Chuang TY; Chen WL; Wang W
    Taiwan J Obstet Gynecol; 2018 Aug; 57(4):583-587. PubMed ID: 30122583
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Unbalanced 15;22 translocation in a patient with manifestations of DiGeorge and velocardiofacial syndrome.
    Jaquez M; Driscoll DA; Li M; Emanuel BS; Hernandez I; Jaquez F; Lembert N; Ramirez J; Matalon R
    Am J Med Genet; 1997 May; 70(1):6-10. PubMed ID: 9129733
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A case of partial trisomy 2p23-pter syndrome with trisomy 18p due to a de novo supernumerary marker chromosome.
    Lee JH; Cho HS; Lee ES; Jung BC
    Korean J Lab Med; 2010 Jun; 30(3):312-7. PubMed ID: 20603594
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Familial Del(18p) syndrome.
    Tsukahara M; Imaizumi K; Fujita K; Tateishi H; Uchida M
    Am J Med Genet; 2001 Feb; 99(1):67-9. PubMed ID: 11170097
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Mosaic rearrangement of chromosome 18: characterization by FISH mapping and DNA studies shows trisomy 18p and monosomy 18p both of paternal origin.
    Oner G; Jauch A; Eggermann T; Hardwick R; Kirsch S; Schiebel K; Rappold G; Robson L; Smith A
    Am J Med Genet; 2000 May; 92(2):101-6. PubMed ID: 10797432
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Subtelomeric chromosomal rearrangements detected in patients with idiopathic mental retardation and dysmorphic features.
    Caliskan MO; Karauzum SB; Mihci E; Tacoy S; Luleci G
    Genet Couns; 2005; 16(2):129-38. PubMed ID: 16080292
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mild phenotypic manifestations of terminal deletion of the long arm of chromosome 4: clinical description of a new patient.
    Caliebe A; Waltz S; Jenderny J
    Clin Genet; 1997 Aug; 52(2):116-9. PubMed ID: 9298747
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 46,XY del(18)(q21.3q22.2) with mosaicism of r(18) and a milder form of the 18q- syndrome.
    Maaswinkel-Mooij PD; de Jong P; Beverstock GC
    Clin Genet; 1993 Feb; 43(2):76-8. PubMed ID: 8448905
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Autopsy findings of a 37-year-old man with a complex mosaic karyotype involving del(18p), monosomy 13, and trisomy 20.
    Halushka MK; Stetten G; McMichael JL; Blakemore KJ; Hutchins GM
    Am J Med Genet A; 2005 Jun; 135(2):181-5. PubMed ID: 15832358
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Emanuel Syndrome (ES): new case-report and review of the literature.
    Jancevska S; Kitanovski M; Laban N; Danilovski D; Tasic V; Gucev ZS
    Pril (Makedon Akad Nauk Umet Odd Med Nauki); 2015; 36(1):205-8. PubMed ID: 26076791
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Chromosome 18 aberrations and epilepsy: a review.
    Grosso S; Pucci L; Di Bartolo RM; Gobbi G; Bartalini G; Anichini C; Scarinci R; Balestri M; Farnetani MA; Cioni M; Morgese G; Balestri P
    Am J Med Genet A; 2005 Apr; 134A(1):88-94. PubMed ID: 15690352
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Craniofacial and Neurological Phenotype in a Patient with De Novo 18q Microdeletion and 18p Microduplication.
    Yapijakis C; Angelopoulou A; Manolakos E; Voumvourakis C
    Adv Exp Med Biol; 2020; 1195():163-166. PubMed ID: 32468472
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Cytogenetic Studies of Rwandan Pediatric Patients Presenting with Global Developmental Delay, Intellectual Disability and/or Multiple Congenital Anomalies.
    Uwineza A; Hitayezu J; Jamar M; Caberg JH; Murorunkwere S; Janvier N; Bours V; Mutesa L
    J Trop Pediatr; 2016 Feb; 62(1):38-45. PubMed ID: 26507407
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Partial trisomy of chromosome 18 (pter----q12) following a familial 18;21 translocation rcp(18;21)(q12;q11).
    Binkert F; Stranzinger J; Schinzel A
    Hum Hered; 1990; 40(2):81-4. PubMed ID: 2335369
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.