BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

874 related articles for article (PubMed ID: 26174853)

  • 1. Haploinsufficiency and triploinsensitivity of the same 6p25.1p24.3 region in a family.
    Qi Z; Jeng LJ; Slavotinek A; Yu J
    BMC Med Genomics; 2015 Jul; 8():38. PubMed ID: 26174853
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genomic findings in patients with clinical suspicion of 22q11.2 deletion syndrome.
    Koczkowska M; Wierzba J; Śmigiel R; Sąsiadek M; Cabała M; Ślężak R; Iliszko M; Kardaś I; Limon J; Lipska-Ziętkiewicz BS
    J Appl Genet; 2017 Feb; 58(1):93-98. PubMed ID: 27629806
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Subtelomeric 6p25 deletion/duplication: Report of a patient with new clinical findings and genotype-phenotype correlations.
    Linhares ND; Svartman M; Rodrigues TC; Rosenberg C; Valadares ER
    Eur J Med Genet; 2015 May; 58(5):310-8. PubMed ID: 25817395
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Array-CGH and clinical characterization in a patient with subtelomeric 6p deletion without ocular dysgenesis.
    Piccione M; Antona R; Salzano E; Cavani S; Malacarne M; Morreale Bubella R; Pierluigi M; Viaggi CD; Corsello G
    Am J Med Genet A; 2012 Jan; 158A(1):150-4. PubMed ID: 22105932
    [TBL] [Abstract][Full Text] [Related]  

  • 5. An interstitial deletion of 7.1Mb in chromosome band 6p22.3 associated with developmental delay and dysmorphic features including heart defects, short neck, and eye abnormalities.
    Bremer A; Schoumans J; Nordenskjöld M; Anderlid BM; Giacobini M
    Eur J Med Genet; 2009; 52(5):358-62. PubMed ID: 19576304
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Prenatal diagnosis of 6pter-p24 deletion syndrome in a fetus from a Han Chinese family: A case report.
    Shi QY; Liu YH; Zhang YS; Yu XW
    Medicine (Baltimore); 2020 Feb; 99(8):e19246. PubMed ID: 32080128
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Ocular developmental abnormalities and glaucoma associated with interstitial 6p25 duplications and deletions.
    Lehmann OJ; Ebenezer ND; Ekong R; Ocaka L; Mungall AJ; Fraser S; McGill JI; Hitchings RA; Khaw PT; Sowden JC; Povey S; Walter MA; Bhattacharya SS; Jordan T
    Invest Ophthalmol Vis Sci; 2002 Jun; 43(6):1843-9. PubMed ID: 12036988
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Clinical characterization of int22h1/int22h2-mediated Xq28 duplication/deletion: new cases and literature review.
    El-Hattab AW; Schaaf CP; Fang P; Roeder E; Kimonis VE; Church JA; Patel A; Cheung SW
    BMC Med Genet; 2015 Mar; 16():12. PubMed ID: 25927380
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Chromosome 6p25 deletion syndrome: report of a case with optic disc coloboma and review of published ophthalmic findings.
    Beby F; Des Portes V; Till M; Mottolese C; Denis P
    Ophthalmic Genet; 2012 Dec; 33(4):240-8. PubMed ID: 22497499
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Novel maternal duplication of 6p22.3-p25.3 with subtelomeric 6p25.3 deletion: new clinical findings and genotype-phenotype correlations.
    Zhang L; Tie X; Che F; Wang G; Ge Y; Li B; Yang Y
    Mol Cytogenet; 2023 Jun; 16(1):11. PubMed ID: 37303060
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Schizophrenia in an adult with 6p25 deletion syndrome.
    Caluseriu O; Mirza G; Ragoussis J; Chow EW; MacCrimmon D; Bassett AS
    Am J Med Genet A; 2006 Jun; 140(11):1208-13. PubMed ID: 16642507
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 6p25 interstitial deletion in two dizygotic twins with gyral pattern anomaly and speech and language disorder.
    Bozza M; Bernardini L; Novelli A; Brovedani P; Moretti E; Canapicchi R; Doccini V; Filippi T; Battaglia A
    Eur J Paediatr Neurol; 2013 May; 17(3):225-31. PubMed ID: 23069351
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Phenotypic and molecular assessment of seven patients with 6p25 deletion syndrome: relevance to ocular dysgenesis and hearing impairment.
    Gould DB; Jaafar MS; Addison MK; Munier F; Ritch R; MacDonald IM; Walter MA
    BMC Med Genet; 2004 Jun; 5():17. PubMed ID: 15219231
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The 6p subtelomere deletion syndrome.
    DeScipio C
    Am J Med Genet C Semin Med Genet; 2007 Nov; 145C(4):377-82. PubMed ID: 17918735
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The phenotypic spectrum of terminal and subterminal 6p deletions based on a social media-derived cohort and literature review.
    Rraku E; Kerstjens-Frederikse WS; Swertz MA; Dijkhuizen T; van Ravenswaaij-Arts CMA; Engwerda A
    Orphanet J Rare Dis; 2023 Mar; 18(1):68. PubMed ID: 36964621
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Recurrent fetal syndromic spina bifida associated with 3q26.1-qter duplication and 5p13.33-pter deletion due to familial balanced rearrangement.
    Preiksaitiene E; Benušienė E; Ciuladaite Z; Šliužas V; Mikštienė V; Kučinskas V
    Taiwan J Obstet Gynecol; 2016 Jun; 55(3):410-4. PubMed ID: 27343325
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 6p subtelomere deletion with congenital glaucoma, severe mental retardation, and growth impairment.
    Nakane T; Kousuke N; Sonoko H; Yuko K; Sato H; Kubota T; Sugita K
    Pediatr Int; 2013 Jun; 55(3):376-81. PubMed ID: 23782370
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Subtelomeric 6p deletion: clinical and array-CGH characterization in two patients.
    Martinet D; Filges I; Besuchet Schmutz N; Morris MA; Gaide AC; Dahoun S; Bottani A; Addor MC; Antonarakis SE; Beckmann JS; Béna F
    Am J Med Genet A; 2008 Aug; 146A(16):2094-102. PubMed ID: 18629875
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Co-occurrence of recurrent duplications of the DiGeorge syndrome region on both chromosome 22 homologues due to inherited and de novo events.
    Bi W; Probst FJ; Wiszniewska J; Plunkett K; Roney EK; Carter BS; Williams MD; Stankiewicz P; Patel A; Stevens CA; Lupski JR; Cheung SW
    J Med Genet; 2012 Nov; 49(11):681-8. PubMed ID: 23042811
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Delineation of two distinct 6p deletion syndromes.
    Davies AF; Mirza G; Sekhon G; Turnpenny P; Leroy F; Speleman F; Law C; van Regemorter N; Vamos E; Flinter F; Ragoussis J
    Hum Genet; 1999 Jan; 104(1):64-72. PubMed ID: 10071194
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 44.