Microarray analysis for constitutional cytogenetic abnormalities
- PMID: 17873655
- DOI: 10.1097/gim.0b013e31814ce3d9
Microarray analysis for constitutional cytogenetic abnormalities
Similar articles
-
Microarray-based prenatal diagnosis for the identification of fetal chromosome abnormalities.Expert Rev Mol Diagn. 2013 Jul;13(6):601-11. doi: 10.1586/14737159.2013.811912. Expert Rev Mol Diagn. 2013. PMID: 23895129 Review.
-
Detection of cryptic pathogenic copy number variations and constitutional loss of heterozygosity using high resolution SNP microarray analysis in 117 patients referred for cytogenetic analysis and impact on clinical practice.J Med Genet. 2009 Feb;46(2):123-31. doi: 10.1136/jmg.2008.062604. Epub 2008 Nov 17. J Med Genet. 2009. PMID: 19015223
-
Prenatal chromosomal microarray analysis in fetuses with congenital heart disease: a prospective cohort study.Am J Obstet Gynecol. 2018 Feb;218(2):244.e1-244.e17. doi: 10.1016/j.ajog.2017.10.225. Epub 2017 Nov 8. Am J Obstet Gynecol. 2018. PMID: 29128521 Clinical Trial.
-
Whole-genome microarray analysis in prenatal specimens identifies clinically significant chromosome alterations without increase in results of unclear significance compared to targeted microarray.Prenat Diagn. 2009 Dec;29(12):1156-66. doi: 10.1002/pd.2371. Prenat Diagn. 2009. PMID: 19795450
-
Genetics of scleroderma: update on single nucleotide polymorphism analysis and microarrays.Curr Opin Rheumatol. 2005 Nov;17(6):761-7. doi: 10.1097/01.bor.0000179943.27777.b1. Curr Opin Rheumatol. 2005. PMID: 16224255 Review.
Cited by
-
Array-based technology and recommendations for utilization in medical genetics practice for detection of chromosomal abnormalities.Genet Med. 2010 Nov;12(11):742-5. doi: 10.1097/GIM.0b013e3181f8baad. Genet Med. 2010. PMID: 20962661 Free PMC article.
-
Clinical implementation of whole-genome array CGH as a first-tier test in 5080 pre and postnatal cases.Mol Cytogenet. 2011 May 9;4:12. doi: 10.1186/1755-8166-4-12. Mol Cytogenet. 2011. PMID: 21549014 Free PMC article.
-
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.J Mol Diagn. 2009 May;11(3):226-37. doi: 10.2353/jmoldx.2009.080064. Epub 2009 Mar 26. J Mol Diagn. 2009. PMID: 19324990 Free PMC article.
-
Expanding diagnostic testing beyond cytogenetics: implications for birth defects research and surveillance.Birth Defects Res A Clin Mol Teratol. 2013 Nov;97(11):726-9. doi: 10.1002/bdra.23195. Epub 2013 Nov 6. Birth Defects Res A Clin Mol Teratol. 2013. PMID: 24265126 Free PMC article. No abstract available.
-
Long-term hypoxic atmosphere enhances the stemness, immunoregulatory functions, and therapeutic application of human umbilical cord mesenchymal stem cells.Bone Joint Res. 2024 Dec 12;13(12):764-778. doi: 10.1302/2046-3758.1312.BJR-2024-0136.R2. Bone Joint Res. 2024. PMID: 39662502 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources