147 related articles for article (PubMed ID: 20942916)
1. MLPA for confirmation of array CGH results and determination of inheritance.
Hills A; Ahn JW; Donaghue C; Thomas H; Mann K; Ogilvie CM
Mol Cytogenet; 2010 Oct; 3():19. PubMed ID: 20942916
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. [Application of array-CGH and MLPA for detection of 4 cryptic unbalanced translocations].
Geng Q; Wu W; Luo F; Xu Z; Chen W; Li F; Xie J
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Jun; 30(3):288-92. PubMed ID: 23744316
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Efficient and cost-effective genetic analysis of products of conception and fetal tissues using a QF-PCR/array CGH strategy; five years of data.
Donaghue C; Davies N; Ahn JW; Thomas H; Ogilvie CM; Mann K
Mol Cytogenet; 2017; 10():12. PubMed ID: 28396697
[TBL] [Abstract][Full Text] [Related]
6. Detection of subtelomere imbalance using MLPA: validation, development of an analysis protocol, and application in a diagnostic centre.
Ahn JW; Ogilvie CM; Welch A; Thomas H; Madula R; Hills A; Donaghue C; Mann K
BMC Med Genet; 2007 Mar; 8():9. PubMed ID: 17338807
[TBL] [Abstract][Full Text] [Related]
7. Analysis of Copy Number Variations in Patients with Autism Using Cytogenetic and MLPA Techniques: Report of 16p13.1p13.3 and 10q26.3 Duplications.
Ghasemi Firouzabadi S; Vameghi R; Kariminejad R; Darvish H; Banihashemi S; Firouzkouhi Moghaddam M; Jamali P; Farbod Mofidi Tehrani H; Dehghani H; Raeisoon MR; Narooie-Nejad M; Jamshidi J; Tafakhori A; Sadabadi S; Behjati F
Int J Mol Cell Med; 2016; 5(4):236-245. PubMed ID: 28357200
[TBL] [Abstract][Full Text] [Related]
8. Multiplex ligation-dependent probe amplification and array comparative genomic hybridization analyses for prenatal diagnosis of cytogenomic abnormalities.
Xu Z; Geng Q; Luo F; Xu F; Li P; Xie J
Mol Cytogenet; 2014; 7(1):84. PubMed ID: 25530804
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Identification of Chromosome Abnormalities in Subtelomeric Regions Using Multiplex Ligation Dependent Probe Amplification (MLPA) Technique in 100 Iranian Patients With Idiopathic Mental Retardation.
Behjati F; Ghasemi Firouzabadi S; Sajedi F; Kahrizi K; Najafi M; Ebrahimizade Ghasemlou B; Shafeghati Y; Behnia F; Mohammadi Arya AR; Karimi H; Hadipour F; Hadipour Z; Jamali P; Kariminejad R; Darvish H; Bahman I; Bagherizadeh E; Najmabadi H; Vameghi R
Iran Red Crescent Med J; 2013 Oct; 15(10):e8221. PubMed ID: 24693374
[TBL] [Abstract][Full Text] [Related]
11. Using a combination of MLPA kits to detect chromosomal imbalances in patients with multiple congenital anomalies and mental retardation is a valuable choice for developing countries.
Jehee FS; Takamori JT; Medeiros PF; Pordeus AC; Latini FR; Bertola DR; Kim CA; Passos-Bueno MR
Eur J Med Genet; 2011; 54(4):e425-32. PubMed ID: 21457803
[TBL] [Abstract][Full Text] [Related]
12. Increased nuchal translucency with normal karyotype: a follow-up study of 100 cases supplemented with CGH and MLPA analyses.
Schou KV; Kirchhoff M; Nygaard U; Jørgensen C; Sundberg K
Ultrasound Obstet Gynecol; 2009 Dec; 34(6):618-22. PubMed ID: 19953565
[TBL] [Abstract][Full Text] [Related]
13. Submicroscopic chromosome imbalance in patients with developmental delay and/or dysmorphism referred specifically for Fragile X testing and karyotype analysis.
Ahn JW; Mann K; Docherty Z; Mackie Ogilvie C
Mol Cytogenet; 2008 Mar; 1():2. PubMed ID: 18471307
[TBL] [Abstract][Full Text] [Related]
14. Evaluation of real-time quantitative PCR as a standard cytogenetic diagnostic tool for confirmation of microarray (aCGH) results and determination of inheritance.
Wang R; Carter J; Lench N
Genet Test Mol Biomarkers; 2013 Nov; 17(11):821-5. PubMed ID: 24024523
[TBL] [Abstract][Full Text] [Related]
15. Detection of cryptic subtelomeric chromosome abnormalities and identification of anonymous chromatin using a quantitative multiplex ligation-dependent probe amplification (MLPA) assay.
Northrop EL; Ren H; Bruno DL; McGhie JD; Coffa J; Schouten J; Choo KH; Slater HR
Hum Mutat; 2005 Nov; 26(5):477-86. PubMed ID: 16170807
[TBL] [Abstract][Full Text] [Related]
16. Evaluation of array comparative genomic hybridization for genetic analysis of chorionic villus sampling from pregnancy loss in comparison to karyotyping and multiplex ligation-dependent probe amplification.
Deshpande M; Harper J; Holloway M; Palmer R; Wang R
Genet Test Mol Biomarkers; 2010 Jun; 14(3):421-4. PubMed ID: 20408732
[TBL] [Abstract][Full Text] [Related]
17. Clinical use of array comparative genomic hybridization (aCGH) for prenatal diagnosis in 300 cases.
Van den Veyver IB; Patel A; Shaw CA; Pursley AN; Kang SH; Simovich MJ; Ward PA; Darilek S; Johnson A; Neill SE; Bi W; White LD; Eng CM; Lupski JR; Cheung SW; Beaudet AL
Prenat Diagn; 2009 Jan; 29(1):29-39. PubMed ID: 19012303
[TBL] [Abstract][Full Text] [Related]
18. Validation and implementation of array comparative genomic hybridisation as a first line test in place of postnatal karyotyping for genome imbalance.
Ahn JW; Mann K; Walsh S; Shehab M; Hoang S; Docherty Z; Mohammed S; Mackie Ogilvie C
Mol Cytogenet; 2010 Apr; 3():9. PubMed ID: 20398301
[TBL] [Abstract][Full Text] [Related]
19. [Genetic and prenatal diagnosis for four families with Williams-Beuren syndrome].
Liu Y; Xu ZY; Wu WQ; Luo FW; Xie JS
Zhongguo Dang Dai Er Ke Za Zhi; 2015 Dec; 17(12):1267-72. PubMed ID: 26695662
[TBL] [Abstract][Full Text] [Related]
20. Customized high resolution CGH-array for clinical diagnosis reveals additional genomic imbalances in previous well-defined pathological samples.
Vallespín E; Palomares Bralo M; Mori MÁ; Martín R; García-Miñaúr S; Fernández L; de Torres ML; García-Santiago F; Mansilla E; Santos F; M-Montaño VE; Crespo MC; Martín S; Martínez-Glez V; Delicado A; Lapunzina P; Nevado J
Am J Med Genet A; 2013 Aug; 161A(8):1950-60. PubMed ID: 23798500
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]