BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

191 related articles for article (PubMed ID: 22413934)

  • 21. Persistent truncus arteriosus in monozygotic twins: case report and literature review.
    Mas C; Delatycki MB; Weintraub RG
    Am J Med Genet; 1999 Jan; 82(2):146-8. PubMed ID: 9934979
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Discordant retinoblastoma in monozygotic twins due to deletion of 13q14.
    Messina-Baas OM; Arroyo-Yllanes ME; Pérez-Pérez JF; González-Huerta LM; Cuevas-Covarrubias SA
    Eur J Ophthalmol; 2014; 24(6):968-71. PubMed ID: 24557757
    [TBL] [Abstract][Full Text] [Related]  

  • 23. A rare mosaic 22q11.2 microdeletion identified in a Chinese family with recurrent fetal conotruncal defects.
    Chen W; Li X; Sun L; Sheng W; Huang G
    Mol Genet Genomic Med; 2019 Aug; 7(8):e847. PubMed ID: 31297990
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Monozygotic twins concordant for Cayler syndrome.
    Rauch A; Hofbeck M; Bähring S; Leipold G; Trautmann U; Singer H; Pfeiffer RA
    Am J Med Genet; 1998 Jan; 75(1):113-7. PubMed ID: 9450869
    [TBL] [Abstract][Full Text] [Related]  

  • 25. A case report of T-box 1 mutation causing phenotypic features of chromosome 22q11.2 deletion syndrome.
    Haddad RA; Clines GA; Wyckoff JA
    Clin Diabetes Endocrinol; 2019; 5():13. PubMed ID: 31428446
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Monozygotic twins concordant for blood karyotype, but phenotypically discordant: a case of "mosaic chimerism".
    Bourthoumieu S; Yardin C; Terro F; Gilbert B; Laroche C; Saura R; Vincent MC; Esclaire F
    Am J Med Genet A; 2005 Jun; 135(2):190-4. PubMed ID: 15832362
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Novel rearrangement of chromosome band 22q11.2 causing 22q11 microdeletion syndrome-like phenotype and rhabdoid tumor of the kidney.
    Wieser R; Fritz B; Ullmann R; Müller I; Galhuber M; Storlazzi CT; Ramaswamy A; Christiansen H; Shimizu N; Rehder H
    Hum Mutat; 2005 Aug; 26(2):78-83. PubMed ID: 15957176
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Mosaic 22q11.2 deletion and tetralogy of Fallot with absent pulmonary valve: an unreported association.
    Prabhu S; Jenny B; James H; Provenzano S
    World J Pediatr Congenit Heart Surg; 2015 Apr; 6(2):342-5. PubMed ID: 25870364
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [Congenital cardiovascular malformations and chromosome microdeletions in 22q11.2].
    Trost D; Engels H; Bauriedel G; Wiebe W; Schwanitz G
    Dtsch Med Wochenschr; 1999 Jan; 124(1-2):3-7. PubMed ID: 9951451
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Monozygotic twins discordant for trisomy 13.
    Ramsey KW; Slavin TP; Graham G; Hirata GI; Balaraman V; Seaver LH
    J Perinatol; 2012 Apr; 32(4):306-8. PubMed ID: 22460600
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Postzygotic mosaicism of a novel PTPN11 mutation in monozygotic twins discordant for metachondromatosis.
    Rydzanicz M; Glinkowski W; Walczak A; Koppolu A; Kostrzewa G; Gasperowicz P; Pollak A; Stawiński P; Płoski R
    Am J Med Genet A; 2022 May; 188(5):1482-1487. PubMed ID: 35112464
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Monozygotic twins discordant for homologous Robertsonian translocation trisomy 21 of 46, XX, + 21, der (21;21) (q10; q10) in a twin-to-twin transfusion syndrome, case report.
    Cao D; Sun J; Li N; Li Z; Liu W; Chen M
    BMC Pregnancy Childbirth; 2021 Jan; 21(1):101. PubMed ID: 33516175
    [TBL] [Abstract][Full Text] [Related]  

  • 33. A case report of monozygotic twins with Smith-Magenis syndrome.
    Hicks M; Ferguson S; Bernier F; Lemay JF
    J Dev Behav Pediatr; 2008 Feb; 29(1):42-6. PubMed ID: 18301319
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Effects of smoking on genome-wide DNA methylation profiles: A study of discordant and concordant monozygotic twin pairs.
    van Dongen J; Willemsen G; ; de Geus EJC; Boomsma DI; Neale MC
    Elife; 2023 Aug; 12():. PubMed ID: 37643467
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Consequences of 22q11.2 Microdeletion on the Genome, Individual and Population Levels.
    Karbarz M
    Genes (Basel); 2020 Aug; 11(9):. PubMed ID: 32842603
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Monochorionic twins discordant for mosaic trisomy 14.
    He M; Pepperell JR; Gundogan F; De Paepe ME; Maggio L; Lu S; Kostadinov S; O'Brien B; Delamonte S; Pinar H; Tantravahi U
    Am J Med Genet A; 2014 May; 164A(5):1227-33. PubMed ID: 24458767
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 22q11.2 distal deletion: a recurrent genomic disorder distinct from DiGeorge syndrome and velocardiofacial syndrome.
    Ben-Shachar S; Ou Z; Shaw CA; Belmont JW; Patel MS; Hummel M; Amato S; Tartaglia N; Berg J; Sutton VR; Lalani SR; Chinault AC; Cheung SW; Lupski JR; Patel A
    Am J Hum Genet; 2008 Jan; 82(1):214-21. PubMed ID: 18179902
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Differences in speech and language abilities between children with 22q11.2 deletion syndrome and children with phenotypic features of 22q11.2 deletion syndrome but without microdeletion.
    Rakonjac M; Cuturilo G; Stevanovic M; Jelicic L; Subotic M; Jovanovic I; Drakulic D
    Res Dev Disabil; 2016 Aug; 55():322-9. PubMed ID: 27235769
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Growth of heterokaryotic monozygotic twins discordant for Ullrich-Turner syndrome during the first years of life.
    Rohrer TR; Gassmann KF; Rauch A; Pfeiffer RA; Doerr HG
    Am J Med Genet A; 2004 Apr; 126A(1):78-83. PubMed ID: 15039976
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Chromosome 22q11.2 Deletion Syndrome: A Comprehensive Review of Molecular Genetics in the Context of Multidisciplinary Clinical Approach.
    Szczawińska-Popłonyk A; Schwartzmann E; Chmara Z; Głukowska A; Krysa T; Majchrzycki M; Olejnicki M; Ostrowska P; Babik J
    Int J Mol Sci; 2023 May; 24(9):. PubMed ID: 37176024
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.