368 related articles for article (PubMed ID: 21707460)
1. Oligonucleotide microarrays in constitutional genetic diagnosis.
Keren B; Le Caignec C
Expert Rev Mol Diagn; 2011 Jun; 11(5):521-32. PubMed ID: 21707460
[TBL] [Abstract][Full Text] [Related]
2. Extending the scope of diagnostic chromosome analysis: detection of single gene defects using high-resolution SNP microarrays.
Bruno DL; Stark Z; Amor DJ; Burgess T; Butler K; Corrie S; Francis D; Ganesamoorthy D; Hills L; James PA; O'Rielly D; Oertel R; Savarirayan R; Prabhakara K; Salce N; Slater HR
Hum Mutat; 2011 Dec; 32(12):1500-6. PubMed ID: 21850686
[TBL] [Abstract][Full Text] [Related]
3. SNP array analysis in constitutional and cancer genome diagnostics--copy number variants, genotyping and quality control.
de Leeuw N; Hehir-Kwa JY; Simons A; Geurts van Kessel A; Smeets DF; Faas BH; Pfundt R
Cytogenet Genome Res; 2011; 135(3-4):212-21. PubMed ID: 21934286
[TBL] [Abstract][Full Text] [Related]
4. Array-based approaches in prenatal diagnosis.
Brady PD; Devriendt K; Deprest J; Vermeesch JR
Methods Mol Biol; 2012; 838():151-71. PubMed ID: 22228011
[TBL] [Abstract][Full Text] [Related]
5. The clinical utility of molecular karyotyping using high-resolution array-comparative genomic hybridization.
Tzetis M; Kitsiou-Tzeli S; Frysira H; Xaidara A; Kanavakis E
Expert Rev Mol Diagn; 2012 Jun; 12(5):449-57. PubMed ID: 22702362
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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]
8. High-resolution molecular karyotyping in patients with developmental delay and/or multiple congenital anomalies in a clinical setting.
Wincent J; Anderlid BM; Lagerberg M; Nordenskjöld M; Schoumans J
Clin Genet; 2011 Feb; 79(2):147-57. PubMed ID: 20486943
[TBL] [Abstract][Full Text] [Related]
9. [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]
10. Copy number imbalances detected with a BAC-based array comparative genomic hybridization platform in congenital diaphragmatic hernia fetuses.
Machado IN; Heinrich JK; Barini R; Peralta CF
Genet Mol Res; 2011 Feb; 10(1):261-7. PubMed ID: 21341218
[TBL] [Abstract][Full Text] [Related]
11. Microdeletion and microduplication syndromes.
Vissers LE; Stankiewicz P
Methods Mol Biol; 2012; 838():29-75. PubMed ID: 22228006
[TBL] [Abstract][Full Text] [Related]
12. ACMG Standards and Guidelines for constitutional cytogenomic microarray analysis, including postnatal and prenatal applications: revision 2013.
South ST; Lee C; Lamb AN; Higgins AW; Kearney HM;
Genet Med; 2013 Nov; 15(11):901-9. PubMed ID: 24071793
[TBL] [Abstract][Full Text] [Related]
13. SNP arrays: comparing diagnostic yields for four platforms in children with developmental delay.
D'Amours G; Langlois M; Mathonnet G; Fetni R; Nizard S; Srour M; Tihy F; Phillips MS; Michaud JL; Lemyre E
BMC Med Genomics; 2014 Dec; 7():70. PubMed ID: 25539807
[TBL] [Abstract][Full Text] [Related]
14. Genomic microarrays: a technology overview.
Brady PD; Vermeesch JR
Prenat Diagn; 2012 Apr; 32(4):336-43. PubMed ID: 22467164
[TBL] [Abstract][Full Text] [Related]
15. Structural genomic variation in intellectual disability.
Pfundt R; Veltman JA
Methods Mol Biol; 2012; 838():77-95. PubMed ID: 22228007
[TBL] [Abstract][Full Text] [Related]
16. Special report: aCGH for the genetic evaluation of patients with developmental delay/mental retardation or autism spectrum disorder.
Technol Eval Cent Assess Program Exec Summ; 2009 Apr; 23(10):1-5. PubMed ID: 19824216
[No Abstract] [Full Text] [Related]
17. 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]
18. Copy-number changes in prenatal diagnosis.
Strassberg M; Fruhman G; Van den Veyver IB
Expert Rev Mol Diagn; 2011 Jul; 11(6):579-92. PubMed ID: 21745012
[TBL] [Abstract][Full Text] [Related]
19. Oligonucleotide microarrays for clinical diagnosis of copy number variation.
Miller DT; Shen Y; Wu BL
Curr Protoc Hum Genet; 2008 Jul; Chapter 8():Unit 8.12. PubMed ID: 18633976
[TBL] [Abstract][Full Text] [Related]
20. [Current limitations and difficulties in application of microarray comparative genomic hybridization in prenatal diagnosis].
Chen Y; Choy KW
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Feb; 28(1):47-51. PubMed ID: 21287509
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
