93 related articles for article (PubMed ID: 31302230)
1. Quantitative PCR evaluation of deletions/duplications identified by array CGH.
Baldan F; Passon N; Burra S; Demori E; Russo PD; Damante G
Mol Cell Probes; 2019 Aug; 46():101421. PubMed ID: 31302230
[TBL] [Abstract][Full Text] [Related]
2. Diagnosis of copy number variation by Illumina next generation sequencing is comparable in performance to oligonucleotide array comparative genomic hybridisation.
Hayes JL; Tzika A; Thygesen H; Berri S; Wood HM; Hewitt S; Pendlebury M; Coates A; Willoughby L; Watson CM; Rabbitts P; Roberts P; Taylor GR
Genomics; 2013 Sep; 102(3):174-81. PubMed ID: 23598253
[TBL] [Abstract][Full Text] [Related]
3. Microarray-based comparative genomic hybridization using sex-matched reference DNA provides greater sensitivity for detection of sex chromosome imbalances than array-comparative genomic hybridization with sex-mismatched reference DNA.
Yatsenko SA; Shaw CA; Ou Z; Pursley AN; Patel A; Bi W; Cheung SW; Lupski JR; Chinault AC; Beaudet AL
J Mol Diagn; 2009 May; 11(3):226-37. PubMed ID: 19324990
[TBL] [Abstract][Full Text] [Related]
4. Quantitative real-time polymerase chain reaction for the verification of genomic imbalances detected by microarray-based comparative genomic hybridization.
Yu S; Kielt M; Stegner AL; Kibiryeva N; Bittel DC; Cooley LD
Genet Test Mol Biomarkers; 2009 Dec; 13(6):751-60. PubMed ID: 20001581
[TBL] [Abstract][Full Text] [Related]
5. Detection of genomic imbalances by array based comparative genomic hybridisation in fetuses with multiple malformations.
Le Caignec C; Boceno M; Saugier-Veber P; Jacquemont S; Joubert M; David A; Frebourg T; Rival JM
J Med Genet; 2005 Feb; 42(2):121-8. PubMed ID: 15689449
[TBL] [Abstract][Full Text] [Related]
6. Clonal heterogeneity in childhood myelodysplastic syndromes--challenge for the detection of chromosomal imbalances by array-CGH.
Praulich I; Tauscher M; Göhring G; Glaser S; Hofmann W; Feurstein S; Flotho C; Lichter P; Niemeyer CM; Schlegelberger B; Steinemann D
Genes Chromosomes Cancer; 2010 Oct; 49(10):885-900. PubMed ID: 20589934
[TBL] [Abstract][Full Text] [Related]
7. Use of Array Comparative Genomic Hybridization for the Diagnosis of DiGeorge Syndrome in Saudi Arabian Population.
Bahamat AA; Assidi M; Lary SA; Almughamsi MM; Peer Zada AA; Chaudhary A; Abuzenadah A; Abu-Elmagd M; Al-Qahtani M
Cytogenet Genome Res; 2018; 154(1):20-29. PubMed ID: 29455205
[TBL] [Abstract][Full Text] [Related]
8. Detection limit of intragenic deletions with targeted array comparative genomic hybridization.
Askree SH; Chin EL; Bean LH; Coffee B; Tanner A; Hegde M
BMC Genet; 2013 Dec; 14():116. PubMed ID: 24304607
[TBL] [Abstract][Full Text] [Related]
9. Targeted array CGH as a valuable molecular diagnostic approach: experience in the diagnosis of mitochondrial and metabolic disorders.
Wang J; Zhan H; Li FY; Pursley AN; Schmitt ES; Wong LJ
Mol Genet Metab; 2012 Jun; 106(2):221-30. PubMed ID: 22494545
[TBL] [Abstract][Full Text] [Related]
10. Comparison of chromosomal and array-based comparative genomic hybridization for the detection of genomic imbalances in primary prostate carcinomas.
Ribeiro FR; Henrique R; Hektoen M; Berg M; Jerónimo C; Teixeira MR; Lothe RA
Mol Cancer; 2006 Sep; 5():33. PubMed ID: 16952311
[TBL] [Abstract][Full Text] [Related]
11. Analysis of genomic alterations in neuroblastoma by multiplex ligation-dependent probe amplification and array comparative genomic hybridization: a comparison of results.
Combaret V; Iacono I; Bréjon S; Schleiermacher G; Pierron G; Couturier J; Bergeron C; Blay JY
Cancer Genet; 2012 Dec; 205(12):657-64. PubMed ID: 23265803
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Detection and calibration of microdeletions and microduplications by array-based comparative genomic hybridization and its applicability to clinical genetic testing.
Wong A; Lese Martin C; Heretis K; Ruffalo T; Wilber K; King W; Ledbetter DH
Genet Med; 2005 Apr; 7(4):264-71. PubMed ID: 15834244
[TBL] [Abstract][Full Text] [Related]
14. Construction and application of a full-coverage, high-resolution, human chromosome 8q genomic microarray for comparative genomic hybridization.
van Duin M; van Marion R; Watson JE; Paris PL; Lapuk A; Brown N; Oseroff VV; Albertson DG; Pinkel D; de Jong P; Nacheva EP; Dinjens W; van Dekken H; Collins C
Cytometry A; 2005; 63(1):10-9. PubMed ID: 15619731
[TBL] [Abstract][Full Text] [Related]
15. Validation of multiplex ligation-dependent probe amplification for confirmation of array comparative genomic hybridization.
Jennings LJ; Yu M; Fitzpatrick C; Smith FA
Diagn Mol Pathol; 2011 Sep; 20(3):166-74. PubMed ID: 21817904
[TBL] [Abstract][Full Text] [Related]
16. New insights in the interpretation of array-CGH: autism spectrum disorder and positive family history for intellectual disability predict the detection of pathogenic variants.
Cappuccio G; Vitiello F; Casertano A; Fontana P; Genesio R; Bruzzese D; Ginocchio VM; Mormile A; Nitsch L; Andria G; Melis D
Ital J Pediatr; 2016 Apr; 42():39. PubMed ID: 27072107
[TBL] [Abstract][Full Text] [Related]
17. A Systems Biology Interpretation of Array Comparative Genomic Hybridization (aCGH) Data through Phylogenetics.
Abunimer AN; Salazar J; Noursi DP; Abu-Asab MS
OMICS; 2016 Mar; 20(3):169-79. PubMed ID: 26983023
[TBL] [Abstract][Full Text] [Related]
18. A method for accurate detection of genomic microdeletions using real-time quantitative PCR.
Weksberg R; Hughes S; Moldovan L; Bassett AS; Chow EW; Squire JA
BMC Genomics; 2005 Dec; 6():180. PubMed ID: 16351727
[TBL] [Abstract][Full Text] [Related]
19. [Genomic abnormalities in children with mental retardation and autism: the use of comparative genomic hybridization in situ (HRCGH) and molecular karyotyping with DNA-microchips (array CGH)].
Vorsanova SG; Iurov IIu; Kurinnaia OS; Voinova VIu; Iurov IuB
Zh Nevrol Psikhiatr Im S S Korsakova; 2013; 113(8):46-9. PubMed ID: 24077551
[TBL] [Abstract][Full Text] [Related]
20. Assessment of copy number variations in 120 patients with Poland syndrome.
Vaccari CM; Tassano E; Torre M; Gimelli S; Divizia MT; Romanini MV; Bossi S; Musante I; Valle M; Senes F; Catena N; Bedeschi MF; Baban A; Calevo MG; Acquaviva M; Lerone M; Ravazzolo R; Puliti A
BMC Med Genet; 2016 Nov; 17(1):89. PubMed ID: 27884122
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]