Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Comment
. 2019 Apr;133(4):827-828.
doi: 10.1097/AOG.0000000000003207.

Chromosomal Microarray Analysis Results From Pregnancies With Various Ultrasonographic Anomalies

Affiliations
Comment

Chromosomal Microarray Analysis Results From Pregnancies With Various Ultrasonographic Anomalies

Angie Jelin et al. Obstet Gynecol. 2019 Apr.
No abstract available

PubMed Disclaimer

Conflict of interest statement

Financial Disclosure: The authors did not report any potential conflicts of interest.

Comment in

  • In Reply.
    Sagi-Dain L, Maya I, Singer A, Ben-Shachar S. Sagi-Dain L, et al. Obstet Gynecol. 2019 Apr;133(4):828. doi: 10.1097/AOG.0000000000003208. Obstet Gynecol. 2019. PMID: 30913183 No abstract available.

Comment on

References

    1. Sagi-Dain L, Maya I, Reches A, Frumkin A, Grinshpun-Cohen J, Segel R, et al. Chromosomal microarray analysis results from pregnancies with various ultrasonographic anomalies. Obstet Gynecol 2018; 132:1368–75. - PubMed
    1. Wapner RJ, Martin CL, Levy B, Ballif BC, Eng CM, Zachary JM, et al. Chromosomal microarray versus karyotyping for prenatal diagnosis. N Engl J Med 2012;367:2175–84. - PMC - PubMed
    1. Microarrays and next-generation sequencing technology: the use of advanced genetic diagnostic tools in obstetrics and gynecology. Committee Opinion No. 682. American College of Obstetricians and Gynecologists. Obstet Gynecol 2016;128:e262–8. - PubMed
    1. Palmer E, Speirs H, Taylor PJ. Changing interpretation of chromosomal microarray over time in a community cohort with intellectual disability. Am J Med Genet A 2014;164A:377–85. - PubMed
    1. SoRelle JA, Thodeson DM, Arnold S, Gotway G, Park JY. Clinical utility of reinterpreting previously reported genomic epilepsy test results for pediatric patients. JAMA Pediatr 2018. [Epub ahead of print]. - PMC - PubMed