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 *

126 related articles for article (PubMed ID: 20672349)

  • 1. Evidence for linkage of the bladder exstrophy-epispadias complex on chromosome 4q31.21-22 and 19q13.31-41 from a consanguineous Iranian family.
    Reutter H; Rüschendorf F; Mattheisen M; Draaken M; Bartels E; Hübner N; Hoffmann P; Payabvash S; Saar K; Nöthen MM; Kajbafzadeh AM; Ludwig M
    Birth Defects Res A Clin Mol Teratol; 2010 Sep; 88(9):757-61. PubMed ID: 20672349
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genome-wide linkage scan for bladder exstrophy-epispadias complex.
    Ludwig M; Rüschendorf F; Saar K; Hübner N; Siekmann L; Boyadjiev SA; Reutter H
    Birth Defects Res A Clin Mol Teratol; 2009 Feb; 85(2):174-8. PubMed ID: 19086019
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Genome-wide analysis for micro-aberrations in familial exstrophy of the bladder using array-based comparative genomic hybridization.
    Reutter H; Hoischen A; Ludwig M; Stein R; Radlwimmer B; Engels H; Wolffenbuttel KP; Weber RG
    BJU Int; 2007 Sep; 100(3):646-50. PubMed ID: 17669146
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Bladder exstrophy-epispadias complex.
    Ludwig M; Ching B; Reutter H; Boyadjiev SA
    Birth Defects Res A Clin Mol Teratol; 2009 Jun; 85(6):509-22. PubMed ID: 19161161
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Bladder exstrophy and epispadias complex in sibling: case report and review of literature.
    Kajbafzadeh AM; Tajik P; Payabvash S; Farzan S; Solhpour AR
    Pediatr Surg Int; 2006 Sep; 22(9):767-70. PubMed ID: 16896811
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Clinical and molecular characterization of the bladder exstrophy-epispadias complex: analysis of 232 families.
    Boyadjiev SA; Dodson JL; Radford CL; Ashrafi GH; Beaty TH; Mathews RI; Broman KW; Gearhart JP
    BJU Int; 2004 Dec; 94(9):1337-43. PubMed ID: 15610117
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Bladder exstrophy-epispadias complex: Investigation of suppressor of variegation, enhancer of zeste and Trithorax (SET) as a candidate gene in a large cohort of patients.
    Reutter H; Thauvin-Robinet C; Boemers TM; Rösch WH; Ludwig M
    Scand J Urol Nephrol; 2006; 40(3):221-4. PubMed ID: 16809264
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genome-wide expression profiling of urinary bladder implicates desmosomal and cytoskeletal dysregulation in the bladder exstrophy-epispadias complex.
    Qi L; Chen K; Hur DJ; Yagnik G; Lakshmanan Y; Kotch LE; Ashrafi GH; Martinez-Murillo F; Kowalski J; Naydenov C; Wittler L; Gearhart JP; Draaken M; Reutter H; Ludwig M; Boyadjiev SA
    Int J Mol Med; 2011 Jun; 27(6):755-65. PubMed ID: 21431277
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The Genomic Architecture of Bladder Exstrophy Epispadias Complex.
    Beaman GM; Cervellione RM; Keene D; Reutter H; Newman WG
    Genes (Basel); 2021 Jul; 12(8):. PubMed ID: 34440323
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Seven new cases of familial isolated bladder exstrophy and epispadias complex (BEEC) and review of the literature.
    Reutter H; Shapiro E; Gruen JR
    Am J Med Genet A; 2003 Jul; 120A(2):215-21. PubMed ID: 12833402
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Candidate gene association study implicates p63 in the etiology of nonsyndromic bladder-exstrophy-epispadias complex.
    Qi L; Wang M; Yagnik G; Mattheisen M; Gearhart JP; Lakshmanan Y; Ebert AK; Rösch W; Ludwig M; Draaken M; Reutter H; Boyadjiev SA
    Birth Defects Res A Clin Mol Teratol; 2013 Dec; 97(12):759-63. PubMed ID: 23913486
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Genetic and molecular biological aspects of the bladder exstrophy-epispadias complex (BEEC)].
    Ludwig M; Utsch B; Reutter H
    Urologe A; 2005 Sep; 44(9):1037-8, 1040-4. PubMed ID: 15973548
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Classic bladder exstrophy: Frequent 22q11.21 duplications and definition of a 414 kb phenocritical region.
    Draaken M; Baudisch F; Timmermann B; Kuhl H; Kerick M; Proske J; Wittler L; Pennimpede T; Ebert AK; Rösch W; Stein R; Bartels E; von Lowtzow C; Boemers TM; Herms S; Gearhart JP; Lakshmanan Y; Kockum CC; Holmdahl G; Läckgren G; Nordenskjöld A; Boyadjiev SA; Herrmann BG; Nöthen MM; Ludwig M; Reutter H
    Birth Defects Res A Clin Mol Teratol; 2014 Jun; 100(6):512-7. PubMed ID: 24764164
    [TBL] [Abstract][Full Text] [Related]  

  • 14. No TAP63 promoter mutation is detected in bladder exstrophy-epispadias complex patients.
    Darling T; Mahfuz I; White SJ; Cheng W
    J Pediatr Surg; 2013 Dec; 48(12):2393-400. PubMed ID: 24314177
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 22q11.2 duplications in a UK cohort with bladder exstrophy-epispadias complex.
    Beaman GM; Woolf AS; Cervellione RM; Keene D; Mushtaq I; Urquhart JE; Stuart HM; Newman WG
    Am J Med Genet A; 2019 Mar; 179(3):404-409. PubMed ID: 30628148
    [TBL] [Abstract][Full Text] [Related]  

  • 16. PLAGL1 epimutation and bladder exstrophy: Coincidence or concurrent etiology?
    Kolarova J; Bens S; Ammerpohl O; Hilger AC; Zhang R; Reutter H; Siebert R
    Birth Defects Res A Clin Mol Teratol; 2016 Aug; 106(8):724-8. PubMed ID: 27223093
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Microduplications at 22q11.21 are associated with non-syndromic classic bladder exstrophy.
    Draaken M; Reutter H; Schramm C; Bartels E; Boemers TM; Ebert AK; Rösch W; Schröder A; Stein R; Moebus S; Stienen D; Hoffmann P; Nöthen MM; Ludwig M
    Eur J Med Genet; 2010; 53(2):55-60. PubMed ID: 20060941
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The inheritance of the exstrophy-epispadias complex.
    Shapiro E; Lepor H; Jeffs RD
    J Urol; 1984 Aug; 132(2):308-10. PubMed ID: 6737583
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Genome-wide linkage in three Dutch families maps a locus for abdominal aortic aneurysms to chromosome 19q13.3.
    Van Vlijmen-Van Keulen CJ; Rauwerda JA; Pals G
    Eur J Vasc Endovasc Surg; 2005 Jul; 30(1):29-35. PubMed ID: 15933979
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Isolated bladder exstrophy associated with a de novo 0.9 Mb microduplication on chromosome 19p13.12.
    Draaken M; Mughal SS; Pennimpede T; Wolter S; Wittler L; Ebert AK; Rösch W; Stein R; Bartels E; Schmidt D; Boemers TM; Schmiedeke E; Hoffmann P; Moebus S; Herrmann BG; Nöthen MM; Reutter H; Ludwig M
    Birth Defects Res A Clin Mol Teratol; 2013 Mar; 97(3):133-9. PubMed ID: 23359465
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.