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Discover Pediatric Collections on COVID-19 and Racism and Its Effects on Pediatric Health

American Academy of Pediatrics

A statement of reaffirmation for this policy was published at

  • e20193991
From the American Academy of PediatricsClinical Report

Comprehensive Evaluation of the Child With Intellectual Disability or Global Developmental Delays

John B. Moeschler, Michael Shevell and COMMITTEE ON GENETICS
Pediatrics September 2014, 134 (3) e903-e918; DOI: https://doi.org/10.1542/peds.2014-1839
John B. Moeschler
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Michael Shevell
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Article Information

vol. 134 no. 3 e903-e918
DOI 
https://doi.org/10.1542/peds.2014-1839
PubMed 
25157020

Published By 
American Academy of Pediatrics
Print ISSN 
0031-4005
Online ISSN 
1098-4275
History 
  • Published online September 2, 2014.

Article Versions

  • previous version (August 25, 2014 - 00:07).
  • You are viewing the most recent version of this article.
Copyright & Usage 
Copyright © 2014 by the American Academy of Pediatrics

Author Information

  1. John B. Moeschler, MD, MS, FAAP, FACMG,
  2. Michael Shevell, MDCM, FRCP,
  3. COMMITTEE ON GENETICS
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    Vol. 134, Issue 3
    1 Sep 2014
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    Comprehensive Evaluation of the Child With Intellectual Disability or Global Developmental Delays
    John B. Moeschler, Michael Shevell, COMMITTEE ON GENETICS
    Pediatrics Sep 2014, 134 (3) e903-e918; DOI: 10.1542/peds.2014-1839

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    Comprehensive Evaluation of the Child With Intellectual Disability or Global Developmental Delays
    John B. Moeschler, Michael Shevell, COMMITTEE ON GENETICS
    Pediatrics Sep 2014, 134 (3) e903-e918; DOI: 10.1542/peds.2014-1839
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    • Table of Contents

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    • Article
      • Abstract
      • Intellectual Disability
      • Chromosome Microarray
      • Screening for Inborn Errors of Metabolism
      • Genetic Testing for Mendelian Disorders
      • Male Gender
      • Genetic Testing for Nonspecific XLID
      • Boys With Suspected or Known XLID
      • Female Gender and MECP2 Testing
      • Advances in Diagnostic Imaging
      • Recommended Approach
      • The Shared Evaluation and Care Plan for Limited Access
      • Emerging Technologies
      • Conclusions
      • Lead Authors
      • American Academy of Pediatrics Committee on Genetics, 2013–2014
      • Past Committee Members
      • Contributor
      • Liaisons
      • Staff
      • Footnotes
      • References
    • Figures & Data
    • Info & Metrics
    • Comments

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    • A meta-analysis of the diagnostic sensitivity and clinical utility of genome sequencing, exome sequencing and chromosomal microarray in children with suspected genetic diseases
    • Analytical and Clinical Validity Study of FirstStepDx PLUS: A Chromosomal Microarray Optimized for Patients with Neurodevelopmental Conditions
    • Intellectual Disabilities
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    • Choosing Wisely Canada: The Canadian College of Medical Geneticists (CCMG) list of five items physicians and patients should question
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