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 *

250 related articles for article (PubMed ID: 20635359)

  • 1. Refinement of causative genes in monosomy 1p36 through clinical and molecular cytogenetic characterization of small interstitial deletions.
    Rosenfeld JA; Crolla JA; Tomkins S; Bader P; Morrow B; Gorski J; Troxell R; Forster-Gibson C; Cilliers D; Hislop RG; Lamb A; Torchia B; Ballif BC; Shaffer LG
    Am J Med Genet A; 2010 Aug; 152A(8):1951-9. PubMed ID: 20635359
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Chromosome 1p36 deletions: the clinical phenotype and molecular characterization of a common newly delineated syndrome.
    Shapira SK; McCaskill C; Northrup H; Spikes AS; Elder FF; Sutton VR; Korenberg JR; Greenberg F; Shaffer LG
    Am J Hum Genet; 1997 Sep; 61(3):642-50. PubMed ID: 9326330
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Molecular characterization of a monosomy 1p36 presenting as an Aicardi syndrome phenocopy.
    Bursztejn AC; Bronner M; Peudenier S; Grégoire MJ; Jonveaux P; Nemos C
    Am J Med Genet A; 2009 Nov; 149A(11):2493-500. PubMed ID: 19842196
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Monosomy 1p36 - a multifaceted and still enigmatic syndrome: four clinically diverse cases with shared white matter abnormalities.
    Õiglane-Shlik E; Puusepp S; Talvik I; Vaher U; Rein R; Tammur P; Reimand T; Teek R; Žilina O; Tomberg T; Õunap K
    Eur J Paediatr Neurol; 2014 May; 18(3):338-46. PubMed ID: 24529875
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Prader-Willi-like phenotype: investigation of 1p36 deletion in 41 patients with delayed psychomotor development, hypotonia, obesity and/or hyperphagia, learning disabilities and behavioral problems.
    D'Angelo CS; Da Paz JA; Kim CA; Bertola DR; Castro CI; Varela MC; Koiffmann CP
    Eur J Med Genet; 2006; 49(6):451-60. PubMed ID: 16564757
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Identification of proximal 1p36 deletions using array-CGH: a possible new syndrome.
    Kang SH; Scheffer A; Ou Z; Li J; Scaglia F; Belmont J; Lalani SR; Roeder E; Enciso V; Braddock S; Buchholz J; Vacha S; Chinault AC; Cheung SW; Bacino CA
    Clin Genet; 2007 Oct; 72(4):329-38. PubMed ID: 17850629
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Physical map of 1p36, placement of breakpoints in monosomy 1p36, and clinical characterization of the syndrome.
    Heilstedt HA; Ballif BC; Howard LA; Lewis RA; Stal S; Kashork CD; Bacino CA; Shapira SK; Shaffer LG
    Am J Hum Genet; 2003 May; 72(5):1200-12. PubMed ID: 12687501
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Recurrent interstitial 1p36 deletions: Evidence for germline mosaicism and complex rearrangement breakpoints.
    Gajecka M; Saitta SC; Gentles AJ; Campbell L; Ciprero K; Geiger E; Catherwood A; Rosenfeld JA; Shaikh T; Shaffer LG
    Am J Med Genet A; 2010 Dec; 152A(12):3074-83. PubMed ID: 21108392
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Loss of the SKI proto-oncogene in individuals affected with 1p36 deletion syndrome is predicted by strain-dependent defects in Ski-/- mice.
    Colmenares C; Heilstedt HA; Shaffer LG; Schwartz S; Berk M; Murray JC; Stavnezer E
    Nat Genet; 2002 Jan; 30(1):106-9. PubMed ID: 11731796
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Del 1p36 syndrome: a newly emerging clinical entity.
    Battaglia A
    Brain Dev; 2005 Aug; 27(5):358-61. PubMed ID: 16023552
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Monosomy 1p36 breakpoint junctions suggest pre-meiotic breakage-fusion-bridge cycles are involved in generating terminal deletions.
    Ballif BC; Yu W; Shaw CA; Kashork CD; Shaffer LG
    Hum Mol Genet; 2003 Sep; 12(17):2153-65. PubMed ID: 12915474
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Phenotypic and Molecular Cytogenetic Analysis of a Case of Monosomy 1p36 Syndrome due to Unbalanced Translocation.
    Hussen DF; Kamel AK; Mekkawy MK; Ashaat EA; El Ruby MO
    Mol Syndromol; 2020 Dec; 11(5-6):284-295. PubMed ID: 33510599
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Extending the phenotype of monosomy 1p36 syndrome and mapping of a critical region for obesity and hyperphagia.
    D'Angelo CS; Kohl I; Varela MC; de Castro CI; Kim CA; Bertola DR; Lourenço CM; Koiffmann CP
    Am J Med Genet A; 2010 Jan; 152A(1):102-10. PubMed ID: 20034100
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Partial monosomy of chromosome 1p36.3: characterization of the critical region and delineation of a syndrome.
    Reish O; Berry SA; Hirsch B
    Am J Med Genet; 1995 Dec; 59(4):467-75. PubMed ID: 8585567
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 576 kb deletion in 1p36.33-p36.32 containing SKI is associated with limb malformation, congenital heart disease and epilepsy.
    Zhu X; Zhang Y; Wang J; Yang JF; Yang YF; Tan ZP
    Gene; 2013 Oct; 528(2):352-5. PubMed ID: 23892090
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Translocation breakpoint mapping and sequence analysis in three monosomy 1p36 subjects with der(1)t(1;1)(p36;q44) suggest mechanisms for telomere capture in stabilizing de novo terminal rearrangements.
    Ballif BC; Wakui K; Gajecka M; Shaffer LG
    Hum Genet; 2004 Jan; 114(2):198-206. PubMed ID: 14579147
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mini-Review: Monosomy 1p36 syndrome: reviewing the correlation between deletion sizes and phenotypes.
    Rocha CF; Vasques RB; Santos SR; Paiva CL
    Genet Mol Res; 2016 Feb; 15(1):. PubMed ID: 26910004
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A girl with 1p36 deletion syndrome and congenital fiber type disproportion myopathy.
    Okamoto N; Toribe Y; Nakajima T; Okinaga T; Kurosawa K; Nonaka I; Shimokawa O; Matsumoto N
    J Hum Genet; 2002; 47(10):556-9. PubMed ID: 12376748
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.