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 *

105 related articles for article (PubMed ID: 23833095)

  • 1. Temporal skin folds in a female infant with an unbalanced translocation with breakpoints Xq22.1 and 6p22.3: a new association?
    Vasileiadis GT; Fordham N; Augustynowicz M; Scott RH
    BMJ Case Rep; 2013 Jul; 2013():. PubMed ID: 23833095
    [No Abstract]   [Full Text] [Related]  

  • 2. Three-way translocation involving band 6q21 in an acute lymphoblastic leukemia.
    Berger R
    Cancer Genet Cytogenet; 2007 Apr; 174(1):74-5. PubMed ID: 17350471
    [No Abstract]   [Full Text] [Related]  

  • 3. Partial trisomy 6p from a de novo translocation (6;18) with variable mosaicism in different tissues.
    Rudnik-Schöneborn S; Schubert R; Majewski F; Haverkamp F; Schwanitz G
    Clin Genet; 1997 Aug; 52(2):126-9. PubMed ID: 9298749
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Subtelomeric 6p monosomy and 12q trisomy in a patient with a 46,XX,der(6)t(6;12)(p25.3;q24.31) karyotype: Phenotypic overlap with Mutchinick syndrome.
    Semerci CN; Cinbis M; Ullmann R; Steininger A; Bahce M; Yagci B; Ozden S; Sabir N; Gumus D; Tepeli E; Arteaga J; Mutchinick OM
    Am J Med Genet A; 2010 Jul; 152A(7):1724-9. PubMed ID: 20578131
    [TBL] [Abstract][Full Text] [Related]  

  • 5. An unbalanced translocation resulting in a duplication of Xq28 causes a Rett syndrome-like phenotype in a female patient.
    Auber B; Burfeind P; Thiels C; Alsat EA; Shoukier M; Liehr T; Nelle H; Bartels I; Salinas-Riester G; Laccone F
    Clin Genet; 2010 Jun; 77(6):593-7. PubMed ID: 20236119
    [No Abstract]   [Full Text] [Related]  

  • 6. Molecular and cytogenetic analysis of the spreading of X inactivation in X;autosome translocations.
    Sharp AJ; Spotswood HT; Robinson DO; Turner BM; Jacobs PA
    Hum Mol Genet; 2002 Dec; 11(25):3145-56. PubMed ID: 12444099
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Partial trisomy 10q with mild phenotype caused by an unbalanced X;10 translocation.
    Mononen T; Sharp A; Laakso M; Meltoranta RL; Valve-Dietz AK; Heinonen K
    J Med Genet; 2003 May; 40(5):e61. PubMed ID: 12746415
    [No Abstract]   [Full Text] [Related]  

  • 8. Unbalanced translocation in an adult patient with premature ovarian failure and mental retardation detected by spectral karyotyping and array-comparative genomic hybridization.
    Guo QS; Qin SY; Zhou SF; He L; Ma D; Zhang YP; Xiong Y; Peng T; Cheng Y; Li XT
    Eur J Clin Invest; 2009 Aug; 39(8):729-37. PubMed ID: 19515099
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Inheritance of a translocation between chromosomes 12 and 16 in a family with recurrent miscarriages and a newborn with Down syndrome carrying the same translocation.
    Pazarbaşi A; Demirhan O; Turgut M; Güzel I; Taştemir D
    Genet Couns; 2008; 19(3):301-8. PubMed ID: 18990986
    [TBL] [Abstract][Full Text] [Related]  

  • 10. An unusual case of retinopathy of prematurity.
    Mandal K; Drury JA; Clark DI
    J Perinatol; 2007 May; 27(5):315-6. PubMed ID: 17453041
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Abnormal sex differentiation and multiple congenital abnormalities in a subject harbouring an apparently balanced (6;8) translocation.
    Ion A; Copin H; Barnoux M; Ajzenberg C; Lesoud A; Cussenot O; Lubetzki J; Telvi L
    J Med Genet; 2000 Dec; 37(12):972-4. PubMed ID: 11186944
    [No Abstract]   [Full Text] [Related]  

  • 12. Miller-Dieker Syndrome with unbalanced translocation 45, X, psu dic(17;Y)(p13;p11.32) detected by fluorescence in situ hybridization and G-banding analysis using high resolution banding technique.
    Mishima T; Watari M; Iwaki Y; Nagai T; Kawamata-Nakamura M; Kobayashi Y; Fujieda S; Oikawa M; Takahashi N; Keira M; Yoshida H; Tonoki H
    Congenit Anom (Kyoto); 2017 Mar; 57(2):61-63. PubMed ID: 27644460
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Recurrent involvement of chromosomal region 6q21 in heterotaxy.
    Peeters H; Debeer P; Groenen P; Van Esch H; Vanderlinden G; Eyskens B; Mertens L; Gewillig M; Van de Ven W; Fryns JP; Devriendt K
    Am J Med Genet; 2001 Sep; 103(1):44-7. PubMed ID: 11562933
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Microphthalmia with linear skin defects syndrome (MIDAS).
    Banganho D; Oliveira I; Machado C; Póvoas M
    BMJ Case Rep; 2019 Apr; 12(4):. PubMed ID: 31015240
    [No Abstract]   [Full Text] [Related]  

  • 15. Spread of X inactivation on chromosome 15 is associated with a more severe phenotype in a girl with an unbalanced t(X; 15) translocation.
    Yeung KS; Chee YY; Luk HM; Kan AS; Tang MH; Lau ET; Shuen AY; Lo IF; Chan KY; Chung BH
    Am J Med Genet A; 2014 Oct; 164A(10):2521-8. PubMed ID: 25044945
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Anterior chamber eye anomalies, redundant skin and syndactyly--a new syndrome associated with breakpoints at 2q37.2 and 7q36.3.
    Temple IK; Browne C; Hodgkins P
    Clin Dysmorphol; 1999 Jul; 8(3):157-63. PubMed ID: 10457847
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Cryptic t(X;18), ins(6;18), and SYT-SSX2 gene fusion in a case of intraneural monophasic synovial sarcoma.
    Lestou VS; O'Connell JX; Robichaud M; Salski C; Mathers J; Maguire J; Chudoba I; Sorensen PH; Lam W; Horsman DE
    Cancer Genet Cytogenet; 2002 Oct; 138(2):153-6. PubMed ID: 12505262
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Attenuated phenotype in a child with trisomy for 1q due to unbalanced X;1 translocation [46,X,der(X),t(X;1)(q28;q32.1)].
    Yatsenko SA; Sahoo T; Rosenkranz M; Mendoza-Londono R; Naeem R; Scaglia F
    Am J Med Genet A; 2004 Jul; 128A(1):72-7. PubMed ID: 15211662
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Association of acute neutrophilic dermatosis and myelodysplastic syndrome with (6; 9) chromosome translocation: a case report and review of the literature.
    Mégarbane B; Bodemer C; Valensi F; Radford-Weiss I; Fraitag S; MacIntyre E; Bletry O; Varet B; Hermine O
    Br J Dermatol; 2000 Dec; 143(6):1322-4. PubMed ID: 11122045
    [No Abstract]   [Full Text] [Related]  

  • 20. Analysis of balanced rearrangements of chromosome 6 in acute leukemia: clustered breakpoints in q22-q23 and possible involvement of c-MYB in a new recurrent translocation, t(6;7)(q23;q32 through 36).
    Sinclair P; Harrison CJ; Jarosová M; Foroni L
    Haematologica; 2005 May; 90(5):602-11. PubMed ID: 15921375
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.