BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

108 related articles for article (PubMed ID: 21950800)

  • 21. Chromosome 22q13.3 deletion syndrome with a de novo interstitial 22q13.3 cryptic deletion disrupting SHANK3.
    Delahaye A; Toutain A; Aboura A; Dupont C; Tabet AC; Benzacken B; Elion J; Verloes A; Pipiras E; Drunat S
    Eur J Med Genet; 2009; 52(5):328-32. PubMed ID: 19454329
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 6q subtelomeric deletion: is there a recognizable syndrome?
    Stevenson DA; Brothman AR; Carey JC; Chen Z; Dent KM; Bale JF; Longo N
    Clin Dysmorphol; 2004 Apr; 13(2):103-106. PubMed ID: 15057127
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Complex constitutional subtelomeric 1p36.3 deletion/duplication in a mentally retarded child with neonatal neuroblastoma.
    Isidor B; Le Cunff M; Boceno M; Boisseau P; Thomas C; Rival JM; David A; Le Caignec C
    Eur J Med Genet; 2008; 51(6):679-84. PubMed ID: 18672103
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Interstitial 6q25 microdeletion syndrome: ARID1B is the key gene.
    Ronzoni L; Tagliaferri F; Tucci A; Baccarin M; Esposito S; Milani D
    Am J Med Genet A; 2016 May; 170A(5):1257-61. PubMed ID: 26754677
    [TBL] [Abstract][Full Text] [Related]  

  • 25. A 1 Mb de novo deletion within 11q13.1q13.2 in a boy with mild intellectual disability and minor dysmorphic features.
    Floor K; Barøy T; Misceo D; Kanavin OJ; Fannemel M; Frengen E
    Eur J Med Genet; 2012 Dec; 55(12):695-9. PubMed ID: 22986108
    [TBL] [Abstract][Full Text] [Related]  

  • 26. A variant Cri du Chat phenotype and autism spectrum disorder in a subject with de novo cryptic microdeletions involving 5p15.2 and 3p24.3-25 detected using whole genomic array CGH.
    Harvard C; Malenfant P; Koochek M; Creighton S; Mickelson EC; Holden JJ; Lewis ME; Rajcan-Separovic E
    Clin Genet; 2005 Apr; 67(4):341-51. PubMed ID: 15733271
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Cloning and characterization of the common fragile site FRA6F harboring a replicative senescence gene and frequently deleted in human tumors.
    Morelli C; Karayianni E; Magnanini C; Mungall AJ; Thorland E; Negrini M; Smith DI; Barbanti-Brodano G
    Oncogene; 2002 Oct; 21(47):7266-76. PubMed ID: 12370818
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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]  

  • 29. Developmental delay and facial dysmorphism in a child with an 8.9 Mb de novo interstitial deletion of 3q25.1-q25.32: Genotype-phenotype correlations of chromosome 3q25 deletion syndrome.
    Moortgat S; Verellen-Dumoulin C; Maystadt I; Parmentier B; Grisart B; Hennecker JL; Destree A
    Eur J Med Genet; 2011; 54(2):177-80. PubMed ID: 21167329
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Regional deletion and amplification on chromosome 6 in a uveal melanoma case without abnormalities on chromosomes 1p, 3 and 8.
    van Gils W; Kilic E; Brüggenwirth HT; Vaarwater J; Verbiest MM; Beverloo B; van Til-Berg ME; Paridaens D; Luyten GP; de Klein A
    Melanoma Res; 2008 Feb; 18(1):10-5. PubMed ID: 18227702
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Interstitial deletion of the long arm of chromosome 6 associated with absent pulmonary valve.
    Horigome H; Takano T; Hirano T; Kajima T; Ohtani S
    Am J Med Genet; 1991 Mar; 38(4):608-11. PubMed ID: 2063905
    [TBL] [Abstract][Full Text] [Related]  

  • 32. New insights into the phenotypes of 6q deletions.
    Hopkin RJ; Schorry E; Bofinger M; Milatovich A; Stern HJ; Jayne C; Saal HM
    Am J Med Genet; 1997 Jun; 70(4):377-86. PubMed ID: 9182778
    [TBL] [Abstract][Full Text] [Related]  

  • 33. A fluorescence in situ hybridization map of 6q deletions in acute lymphocytic leukemia: identification and analysis of a candidate tumor suppressor gene.
    Sinclair PB; Sorour A; Martineau M; Harrison CJ; Mitchell WA; O'Neill E; Foroni L
    Cancer Res; 2004 Jun; 64(12):4089-98. PubMed ID: 15205317
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Characterization of FRA6E and its potential role in autosomal recessive juvenile parkinsonism and ovarian cancer.
    Denison SR; Callahan G; Becker NA; Phillips LA; Smith DI
    Genes Chromosomes Cancer; 2003 Sep; 38(1):40-52. PubMed ID: 12874785
    [TBL] [Abstract][Full Text] [Related]  

  • 35. An epileptic case with mosaic ring chromosome 6 and 6q terminal deletion.
    Kara N; Okten G; Guneş SO; Saglam Y; Tasdemir HA; Pinarli FA
    Epilepsy Res; 2008 Aug; 80(2-3):219-23. PubMed ID: 18485670
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Disruption of the gene Euchromatin Histone Methyl Transferase1 (Eu-HMTase1) is associated with the 9q34 subtelomeric deletion syndrome.
    Kleefstra T; Smidt M; Banning MJ; Oudakker AR; Van Esch H; de Brouwer AP; Nillesen W; Sistermans EA; Hamel BC; de Bruijn D; Fryns JP; Yntema HG; Brunner HG; de Vries BB; van Bokhoven H
    J Med Genet; 2005 Apr; 42(4):299-306. PubMed ID: 15805155
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 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]  

  • 38. 6q25.1-q25.3 Microdeletion in a Chinese Girl.
    Zhong ML; Song YM; Zou CC
    J Clin Res Pediatr Endocrinol; 2021 Feb; 13(1):109-113. PubMed ID: 32380822
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Chromosome 5q subtelomeric deletion syndrome.
    Rauch A; Dörr HG
    Am J Med Genet C Semin Med Genet; 2007 Nov; 145C(4):372-6. PubMed ID: 17910075
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Monosomy 1p36 deletion syndrome.
    Gajecka M; Mackay KL; Shaffer LG
    Am J Med Genet C Semin Med Genet; 2007 Nov; 145C(4):346-56. PubMed ID: 17918734
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.