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 *

194 related articles for article (PubMed ID: 22086107)

  • 41. Array-CGH analysis in Rwandan patients presenting development delay/intellectual disability with multiple congenital anomalies.
    Uwineza A; Caberg JH; Hitayezu J; Hellin AC; Jamar M; Dideberg V; Rusingiza EK; Bours V; Mutesa L
    BMC Med Genet; 2014 Jul; 15():79. PubMed ID: 25016475
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Evaluation of the efficacy of constitutional array-based comparative genomic hybridization in the diagnosis of aneuploidy using genomic and amplified DNA.
    Tan NH; Palmer R; Wang R
    J Obstet Gynaecol Res; 2010 Feb; 36(1):19-26. PubMed ID: 20178523
    [TBL] [Abstract][Full Text] [Related]  

  • 43. High frequency of submicroscopic genomic aberrations detected by tiling path array comparative genome hybridisation in patients with isolated congenital heart disease.
    Erdogan F; Larsen LA; Zhang L; Tümer Z; Tommerup N; Chen W; Jacobsen JR; Schubert M; Jurkatis J; Tzschach A; Ropers HH; Ullmann R
    J Med Genet; 2008 Nov; 45(11):704-9. PubMed ID: 18713793
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Whole-genome array CGH identifies pathogenic copy number variations in fetuses with major malformations and a normal karyotype.
    D'Amours G; Kibar Z; Mathonnet G; Fetni R; Tihy F; Désilets V; Nizard S; Michaud JL; Lemyre E
    Clin Genet; 2012 Feb; 81(2):128-41. PubMed ID: 21496010
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Interpretation of clinical relevance of X-chromosome copy number variations identified in a large cohort of individuals with cognitive disorders and/or congenital anomalies.
    Willemsen MH; de Leeuw N; de Brouwer AP; Pfundt R; Hehir-Kwa JY; Yntema HG; Nillesen WM; de Vries BB; van Bokhoven H; Kleefstra T
    Eur J Med Genet; 2012 Nov; 55(11):586-98. PubMed ID: 22796527
    [TBL] [Abstract][Full Text] [Related]  

  • 46. [Fetal chromosome technique by microarray-based comparative genomic hybridization].
    Jonveaux P
    Arch Pediatr; 2010 Jul; 17(7):1119-23. PubMed ID: 20347579
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Array-based comparative genomic hybridization of mapped BAC DNA clones to screen for chromosome 14 copy number abnormalities in meningiomas.
    Espinosa AB; Mackintosh C; Maíllo A; Gutierrez L; Sousa P; Merino M; Ortiz J; de Alava E; Orfao A; Tabernero MD
    Eur J Hum Genet; 2008 Dec; 16(12):1450-8. PubMed ID: 18628790
    [TBL] [Abstract][Full Text] [Related]  

  • 48. An interstitial deletion of 7.1Mb in chromosome band 6p22.3 associated with developmental delay and dysmorphic features including heart defects, short neck, and eye abnormalities.
    Bremer A; Schoumans J; Nordenskjöld M; Anderlid BM; Giacobini M
    Eur J Med Genet; 2009; 52(5):358-62. PubMed ID: 19576304
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Genome arrays for the detection of copy number variations in idiopathic mental retardation, idiopathic generalized epilepsy and neuropsychiatric disorders: lessons for diagnostic workflow and research.
    Hochstenbach R; Buizer-Voskamp JE; Vorstman JA; Ophoff RA
    Cytogenet Genome Res; 2011; 135(3-4):174-202. PubMed ID: 22056632
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Detection of pathogenic gene copy number variations in patients with mental retardation by genomewide oligonucleotide array comparative genomic hybridization.
    Fan YS; Jayakar P; Zhu H; Barbouth D; Sacharow S; Morales A; Carver V; Benke P; Mundy P; Elsas LJ
    Hum Mutat; 2007 Nov; 28(11):1124-32. PubMed ID: 17621639
    [TBL] [Abstract][Full Text] [Related]  

  • 51. The frequency of CNVs in a cohort population of consecutive fetuses with congenital anomalies after the termination of pregnancy.
    Rudolf G; Lovrečić L; Tul N; Teran N; Peterlin B
    Mol Genet Genomic Med; 2019 Jun; 7(6):e658. PubMed ID: 31004418
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Large-scale copy number variants (CNVs) detected in different ethnic human populations.
    Takahashi N; Satoh Y; Kodaira M; Katayama H
    Cytogenet Genome Res; 2008; 123(1-4):224-33. PubMed ID: 19287159
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Genomic alterations of chromosome region 11p as predictive marker by array comparative genomic hybridization in lung adenocarcinoma patients.
    Sung JS; Park KH; Kim YH
    Cancer Genet Cytogenet; 2010 Apr; 198(1):27-34. PubMed ID: 20303011
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Prematurity, ventricular septal defect and dysmorphisms are independent predictors of pathogenic copy number variants: a retrospective study on array-CGH results and phenotypical features of 293 children with neurodevelopmental disorders and/or multiple congenital anomalies.
    Maini I; Ivanovski I; Djuric O; Caraffi SG; Errichiello E; Marinelli M; Franchi F; Bizzarri V; Rosato S; Pollazzon M; Gelmini C; Malacarne M; Fusco C; Gargano G; Bernasconi S; Zuffardi O; Garavelli L
    Ital J Pediatr; 2018 Mar; 44(1):34. PubMed ID: 29523172
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Practical guidelines for interpreting copy number gains detected by high-resolution array in routine diagnostics.
    Hanemaaijer NM; Sikkema-Raddatz B; van der Vries G; Dijkhuizen T; Hordijk R; van Essen AJ; Veenstra-Knol HE; Kerstjens-Frederikse WS; Herkert JC; Gerkes EH; Leegte LK; Kok K; Sinke RJ; van Ravenswaaij-Arts CM
    Eur J Hum Genet; 2012 Feb; 20(2):161-5. PubMed ID: 21934709
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Clinical laboratory implementation of cytogenomic microarrays.
    South ST; Brothman AR
    Cytogenet Genome Res; 2011; 135(3-4):203-11. PubMed ID: 21934287
    [TBL] [Abstract][Full Text] [Related]  

  • 57. High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays.
    Pinkel D; Segraves R; Sudar D; Clark S; Poole I; Kowbel D; Collins C; Kuo WL; Chen C; Zhai Y; Dairkee SH; Ljung BM; Gray JW; Albertson DG
    Nat Genet; 1998 Oct; 20(2):207-11. PubMed ID: 9771718
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Sporadic male patients with intellectual disability: contribution of X-chromosome copy number variants.
    Isrie M; Froyen G; Devriendt K; de Ravel T; Fryns JP; Vermeesch JR; Van Esch H
    Eur J Med Genet; 2012 Nov; 55(11):577-85. PubMed ID: 22659343
    [TBL] [Abstract][Full Text] [Related]  

  • 59. A homozygous deletion of a normal variation locus in a patient with hearing loss from non-consanguineous parents.
    Knijnenburg J; Oberstein SA; Frei K; Lucas T; Gijsbers AC; Ruivenkamp CA; Tanke HJ; Szuhai K
    J Med Genet; 2009 Jun; 46(6):412-7. PubMed ID: 19246478
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Application of chromosomal microarray in the evaluation of abnormal prenatal findings.
    Yatsenko SA; Davis S; Hendrix NW; Surti U; Emery S; Canavan T; Speer P; Hill L; Clemens M; Rajkovic A
    Clin Genet; 2013 Jul; 84(1):47-54. PubMed ID: 23020214
    [TBL] [Abstract][Full Text] [Related]  

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