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Prevalence of Underdiagnosed Fragile X Syndrome in 2 Health Systems.

Publication ,  Journal Article
Movaghar, A; Page, D; Brilliant, M; Mailick, M
Published in: JAMA Netw Open
December 1, 2021

This cross-sectional study examines the gap between best estimates of prevalence and clinical diagnosis of fragile X syndrome by mining the electronic health records of 3.8 million people in Wisconsin.

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Published In

JAMA Netw Open

DOI

EISSN

2574-3805

Publication Date

December 1, 2021

Volume

4

Issue

12

Start / End Page

e2141516

Location

United States

Related Subject Headings

  • Young Adult
  • Wisconsin
  • Prevalence
  • Middle Aged
  • Male
  • Infant, Newborn
  • Infant
  • Humans
  • Genetic Testing
  • Fragile X Syndrome
 

Citation

APA
Chicago
ICMJE
MLA
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Movaghar, A., Page, D., Brilliant, M., & Mailick, M. (2021). Prevalence of Underdiagnosed Fragile X Syndrome in 2 Health Systems. JAMA Netw Open, 4(12), e2141516. https://doi.org/10.1001/jamanetworkopen.2021.41516
Movaghar, Arezoo, David Page, Murray Brilliant, and Marsha Mailick. “Prevalence of Underdiagnosed Fragile X Syndrome in 2 Health Systems.JAMA Netw Open 4, no. 12 (December 1, 2021): e2141516. https://doi.org/10.1001/jamanetworkopen.2021.41516.
Movaghar A, Page D, Brilliant M, Mailick M. Prevalence of Underdiagnosed Fragile X Syndrome in 2 Health Systems. JAMA Netw Open. 2021 Dec 1;4(12):e2141516.
Movaghar, Arezoo, et al. “Prevalence of Underdiagnosed Fragile X Syndrome in 2 Health Systems.JAMA Netw Open, vol. 4, no. 12, Dec. 2021, p. e2141516. Pubmed, doi:10.1001/jamanetworkopen.2021.41516.
Movaghar A, Page D, Brilliant M, Mailick M. Prevalence of Underdiagnosed Fragile X Syndrome in 2 Health Systems. JAMA Netw Open. 2021 Dec 1;4(12):e2141516.

Published In

JAMA Netw Open

DOI

EISSN

2574-3805

Publication Date

December 1, 2021

Volume

4

Issue

12

Start / End Page

e2141516

Location

United States

Related Subject Headings

  • Young Adult
  • Wisconsin
  • Prevalence
  • Middle Aged
  • Male
  • Infant, Newborn
  • Infant
  • Humans
  • Genetic Testing
  • Fragile X Syndrome