BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

177 related articles for article (PubMed ID: 17551325)

  • 21. Complex MCA/MR syndrome associated with interstitial deletion of the long arm of chromosome 6, del(6)(q25.1-->q27).
    Vermeesch JR; Fryns JP
    Am J Med Genet A; 2003 Jul; 120A(2):299-300. PubMed ID: 12833421
    [No Abstract]   [Full Text] [Related]  

  • 22. 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]  

  • 23. The phenotypic spectrum of terminal 6q deletions based on a large cohort derived from social media and literature: a prominent role for DLL1.
    Engwerda A; Kerstjens-Frederikse WS; Corsten-Janssen N; Dijkhuizen T; van Ravenswaaij-Arts CMA
    Orphanet J Rare Dis; 2023 Mar; 18(1):59. PubMed ID: 36935482
    [TBL] [Abstract][Full Text] [Related]  

  • 24. 6q terminal deletion syndrome associated with a distinctive EEG and clinical pattern: a report of five cases.
    Elia M; Striano P; Fichera M; Gaggero R; Castiglia L; Galesi O; Malacarne M; Pierluigi M; Amato C; Musumeci SA; Romano C; Majore S; Grammatico P; Zara F; Striano S; Faravelli F
    Epilepsia; 2006 May; 47(5):830-8. PubMed ID: 16686647
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Deletion of proximal 6q: a clinical report and review of the literature.
    Yamamoto Y; Okamoto N; Shiraishi H; Yanagisawa M; Kamoshita S
    Am J Med Genet; 1986 Nov; 25(3):467-71. PubMed ID: 3789009
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Haploinsufficiency of the gene Quaking (QKI) is associated with the 6q terminal deletion syndrome.
    Backx L; Fryns JP; Marcelis C; Devriendt K; Vermeesch J; Van Esch H
    Am J Med Genet A; 2010 Feb; 152A(2):319-26. PubMed ID: 20082458
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Deletion of the long arm of chromosome 6: report on a new case with intractable epilepsy.
    Cerminara C; Bombardieri R; Pinci M; Seri S; Curatolo P
    J Child Neurol; 2006 Jun; 21(6):527-31. PubMed ID: 16948941
    [TBL] [Abstract][Full Text] [Related]  

  • 28. A novel interstitial deletion of chromosome 2q21.1-q23.3: Case report and literature review.
    Almuzzaini B; Alatwi NS; Alsaif S; Al Balwi MA
    Mol Genet Genomic Med; 2020 Apr; 8(4):e1135. PubMed ID: 31989799
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Delineation of the interstitial 6q25 microdeletion syndrome: refinement of the critical causative region.
    Michelson M; Ben-Sasson A; Vinkler C; Leshinsky-Silver E; Netzer I; Frumkin A; Kivity S; Lerman-Sagie T; Lev D
    Am J Med Genet A; 2012 Jun; 158A(6):1395-9. PubMed ID: 22585544
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Substantial reduction of the gastric carcinoma critical region at 6q16.3-q23.1.
    Carvalho B; Seruca R; Carneiro F; Buys CH; Kok K
    Genes Chromosomes Cancer; 1999 Sep; 26(1):29-34. PubMed ID: 10441002
    [TBL] [Abstract][Full Text] [Related]  

  • 31. 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]  

  • 32. Delineation of a critical region on chromosome 18 for the del(18)(q12.2q21.1) syndrome.
    Buysse K; Menten B; Oostra A; Tavernier S; Mortier GR; Speleman F
    Am J Med Genet A; 2008 May; 146A(10):1330-4. PubMed ID: 18412119
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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]  

  • 34. Delineation of candidate genes responsible for structural brain abnormalities in patients with terminal deletions of chromosome 6q27.
    Peddibhotla S; Nagamani SC; Erez A; Hunter JV; Holder JL; Carlin ME; Bader PI; Perras HM; Allanson JE; Newman L; Simpson G; Immken L; Powell E; Mohanty A; Kang SH; Stankiewicz P; Bacino CA; Bi W; Patel A; Cheung SW
    Eur J Hum Genet; 2015 Jan; 23(1):54-60. PubMed ID: 24736736
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Isolated 6q terminal deletions: an emerging new syndrome.
    Bertini V; De Vito G; Costa R; Simi P; Valetto A
    Am J Med Genet A; 2006 Jan; 140(1):74-81. PubMed ID: 16329114
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Comparative genomic hybridization reveals a partial de novo trisomy 6q23-qter in an infant with congenital malformations: delineation of the phenotype.
    Erdel M; Duba HC; Verdorfer I; Lingenhel A; Geiger R; Gutenberger KH; Ludescher E; Utermann B; Utermann G
    Hum Genet; 1997 May; 99(5):596-601. PubMed ID: 9150724
    [TBL] [Abstract][Full Text] [Related]  

  • 37. De novo interstitial deletion in the long arm of chromosome 11: a case report.
    Li LL; Zhang HG; Shao XG; Gao JC; Zhang HY; Liu RZ
    Genet Mol Res; 2016 Jul; 15(2):. PubMed ID: 27421024
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Interstitial deletion of 18q: comparative genomic hybridization array analysis of 46, XX,del(18)(q21.2.q21.33).
    Kato Z; Morimoto W; Kimura T; Matsushima A; Kondo N
    Birth Defects Res A Clin Mol Teratol; 2010 Feb; 88(2):132-5. PubMed ID: 19813260
    [TBL] [Abstract][Full Text] [Related]  

  • 39. A detailed investigation of two cases exhibiting characteristics of the 6p deletion syndrome.
    Davies AF; Olavesen MG; Stephens RJ; Davidson R; Delneste D; Van Regemorter N; Vamos E; Flinter F; Abusaad I; Ragoussis J
    Hum Genet; 1996 Oct; 98(4):454-9. PubMed ID: 8792822
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Ophthalmologic abnormalities in a de novo terminal 6q deletion.
    Abu-Amero KK; Hellani A; Salih MA; Al Hussain A; al Obailan M; Zidan G; Alorainy IA; Bosley TM
    Ophthalmic Genet; 2010 Mar; 31(1):1-11. PubMed ID: 20141352
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.