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

American Academy of Pediatrics

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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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Pediatrics
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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Cited By...

  • Bridging the Gap between Scientific Advancement and Real-World Application: Pediatric Genetic Counseling for Common Syndromes and Single-Gene Disorders
  • Genetic Counseling in Neurodevelopmental Disorders
  • Critical exon indexing improves clinical interpretation of copy number variants in neurodevelopmental disorders
  • Managing challenging behaviour in children with possible learning disability
  • 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
  • Soins primaires aux adultes ayant des deficiences intellectuelles et developpementales: Lignes directrices consensuelles canadiennes de 2018
  • Choosing Wisely Canada: The Canadian College of Medical Geneticists (CCMG) list of five items physicians and patients should question
  • A clinical approach to developmental delay and intellectual disability
  • Current evidence-based recommendations on investigating children with global developmental delay
  • Assessing the Fragile X Syndrome Newborn Screening Landscape
  • Public Health Literature Review of Fragile X Syndrome
  • Developmental Milestones
  • Delivery of epilepsy care to adults with intellectual and developmental disabilities
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