BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

144 related articles for article (PubMed ID: 22123463)

  • 21. Inv dup del(10q): identification by fluorescence in situ hybridization and array comparative genomic hybridization in a fetus with two concurrent chromosomal rearrangements.
    Chen CP; Chen M; Su YN; Huang JP; Ma GC; Chang SP; Chern SR; Chen YT; Su JW; Lee CC; Town DD; Wang W
    Taiwan J Obstet Gynecol; 2012 Jun; 51(2):245-52. PubMed ID: 22795102
    [TBL] [Abstract][Full Text] [Related]  

  • 22. The usefulness of array comparative genomic hybridization in clinical diagnostics of intellectual disability in children.
    Bartnik M; Wiśniowiecka-Kowalnik B; Nowakowska B; Smyk M; Kędzior M; Sobecka K; Kutkowska-Kaźmierczak A; Klapecki J; Szczałuba K; Castañeda J; Własienko P; Bezniakow N; Obersztyn E; Bocian E
    Dev Period Med; 2014; 18(3):307-17. PubMed ID: 25182394
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Array-CGH analysis in patients with intellectual disability and/or congenital malformations in Brazil.
    Vianna GS; Medeiros PF; Alves AF; Silva TO; Jehee FS
    Genet Mol Res; 2016 Feb; 15(1):. PubMed ID: 26909975
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [Balanced chromosomal rearrangements resulting in intellectual disability. An analysis of 22 cases with application of CGH and FISH methods].
    Borg K; Bocian E; Bernaciak J; Nowakowska B; Derwińska K; Obersztyn E; Szczałuba K; Smigiel R; Kostyk E; Mazurczak T
    Med Wieku Rozwoj; 2009; 13(2):81-93. PubMed ID: 19837989
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Cytogenomic Evaluation of Children with Congenital Anomalies: Critical Implications for Diagnostic Testing and Genetic Counseling.
    Szczałuba K; Jakubiuk-Tomaszuk A; Kędzior M; Bernaciak J; Zdrodowska J; Kurzątkowski W; Radkowski M; Demkow U
    Adv Exp Med Biol; 2016; 912():11-9. PubMed ID: 26987321
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Clinical and molecular-cytogenetic studies of cryptic chromosome aberrations in individuals with idiopathic mental retardation and multiple congenital malformations.
    Stoeva RE; Grozdanova LI; Vermeesch JR; Kirchhoff M; Fryns JP; Ivanov IS; Patcheva IH; Dimitrov BI; Krastev TB; Linev AJ; Stefanova MT
    Folia Med (Plovdiv); 2008; 50(4):55-62. PubMed ID: 19209531
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Genomic imbalances detected by array-CGH in patients with syndromal ocular developmental anomalies.
    Delahaye A; Bitoun P; Drunat S; Gérard-Blanluet M; Chassaing N; Toutain A; Verloes A; Gatelais F; Legendre M; Faivre L; Passemard S; Aboura A; Kaltenbach S; Quentin S; Dupont C; Tabet AC; Amselem S; Elion J; Gressens P; Pipiras E; Benzacken B
    Eur J Hum Genet; 2012 May; 20(5):527-33. PubMed ID: 22234157
    [TBL] [Abstract][Full Text] [Related]  

  • 28. An oligonucleotide based array-CGH system for detection of genome wide copy number changes including subtelomeric regions for genetic evaluation of mental retardation.
    Toruner GA; Streck DL; Schwalb MN; Dermody JJ
    Am J Med Genet A; 2007 Apr; 143A(8):824-9. PubMed ID: 17366576
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [The diagnostic value of chromosome microarray analysis technique in the genetic causes of children with intellectual disability or global developmental delay].
    Wu HR; Li L; Ma YN; Liu CL; Pei P; Zheng XF; Wang ST; Xiao Y; Bu DF; Xu YF; Pan H; Qi Y
    Zhonghua Yi Xue Za Zhi; 2021 Jan; 101(3):224-228. PubMed ID: 33455150
    [No Abstract]   [Full Text] [Related]  

  • 30. Application of metaphase HR-CGH and targeted Chromosomal Microarray Analyses to genomic characterization of 116 patients with mental retardation and dysmorphic features.
    Nowakowska B; Stankiewicz P; Obersztyn E; Ou Z; Li J; Chinault AC; Smyk M; Borg K; Mazurczak T; Cheung SW; Bocian E
    Am J Med Genet A; 2008 Sep; 146A(18):2361-9. PubMed ID: 18698622
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Array analysis and karyotyping: workflow consequences based on a retrospective study of 36,325 patients with idiopathic developmental delay in the Netherlands.
    Hochstenbach R; van Binsbergen E; Engelen J; Nieuwint A; Polstra A; Poddighe P; Ruivenkamp C; Sikkema-Raddatz B; Smeets D; Poot M
    Eur J Med Genet; 2009; 52(4):161-9. PubMed ID: 19362174
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Clinical utility of array comparative genomic hybridisation for prenatal diagnosis: a cohort study of 3171 pregnancies.
    Lee CN; Lin SY; Lin CH; Shih JC; Lin TH; Su YN
    BJOG; 2012 Apr; 119(5):614-25. PubMed ID: 22313859
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Genome-wide screening of cytogenetic abnormalities in multiple myeloma patients using array-CGH technique: a Czech multicenter experience.
    Smetana J; Frohlich J; Zaoralova R; Vallova V; Greslikova H; Kupska R; Nemec P; Mikulasova A; Almasi M; Pour L; Adam Z; Sandecka V; Zahradová L; Hajek R; Kuglik P
    Biomed Res Int; 2014; 2014():209670. PubMed ID: 24987674
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Use of targeted array-based CGH for the clinical diagnosis of chromosomal imbalance: is less more?
    Bejjani BA; Saleki R; Ballif BC; Rorem EA; Sundin K; Theisen A; Kashork CD; Shaffer LG
    Am J Med Genet A; 2005 Apr; 134(3):259-67. PubMed ID: 15723295
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Diagnostic utility of array-based comparative genomic hybridization in a clinical setting.
    Baris HN; Tan WH; Kimonis VE; Irons MB
    Am J Med Genet A; 2007 Nov; 143A(21):2523-33. PubMed ID: 17910064
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Microarray-based comparative genomic hybridization analysis in neonates with congenital anomalies: detection of chromosomal imbalances.
    Emy Dorfman L; Leite JC; Giugliani R; Riegel M
    J Pediatr (Rio J); 2015; 91(1):59-67. PubMed ID: 25203518
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Analysis of chromosomal abnormalities by CGH-array in patients with dysmorphic and intellectual disability with normal karyotype.
    Pratte-Santos R; Ribeiro KH; Santos TA; Cintra TS
    Einstein (Sao Paulo); 2016; 14(1):30-4. PubMed ID: 27074231
    [TBL] [Abstract][Full Text] [Related]  

  • 38. BAC array CGH reveals genomic aberrations in idiopathic mental retardation.
    Miyake N; Shimokawa O; Harada N; Sosonkina N; Okubo A; Kawara H; Okamoto N; Kurosawa K; Kawame H; Iwakoshi M; Kosho T; Fukushima Y; Makita Y; Yokoyama Y; Yamagata T; Kato M; Hiraki Y; Nomura M; Yoshiura K; Kishino T; Ohta T; Mizuguchi T; Niikawa N; Matsumoto N
    Am J Med Genet A; 2006 Feb; 140(3):205-11. PubMed ID: 16419101
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Cryptic chromosome rearrangements in five patients, with normal and/or abnormal karyotypes, associated with mental retardation, autism and/or epilepsy, detected by BAC genome array-CGH.
    Cabras V; Milia A; Montaldo C; Nucaro A
    Prague Med Rep; 2012; 113(4):279-88. PubMed ID: 23249659
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [Array comparative genomic hybridization detection of a de novo 4q21.21-q22.1 deletion in a child with severe growth retardation].
    Zhou J; Hu P; Liu A; Li L; Ji X; Hui W; Wang Y; Xu Z
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Feb; 31(1):52-5. PubMed ID: 24510563
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.