Underrepresentation of the term cerebral palsy in clinical genetics databases-Reference-Cited by-同舟云学术

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Underrepresentation of the term cerebral palsy in clinical genetics databases

Published:2022-08-12 Issue:12 Volume:188 Page:3555-3557
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:American J of Med Genetics Pt A

Author:

Srivastava Siddharth¹^ORCID,Lewis Sara A.²³⁴⁵⁶,Kruer Michael C.²³⁴⁵⁶,Poduri Annapurna¹

Affiliation:

1. Department of Neurology, Boston Children's Hospital Harvard Medical School Boston Massachusetts USA

2. Pediatric Movement Disorders Program, Barrow Neurological Institute Phoenix Children's Hospital Phoenix Arizona USA

3. Department of Child Health University of Arizona College of Medicine Phoenix Arizona USA

4. Department of Cellular and Molecular Medicine University of Arizona College of Medicine Phoenix Arizona USA

5. Department of Neurology University of Arizona College of Medicine Phoenix Arizona USA

6. Program in Genetics University of Arizona College of Medicine Phoenix Arizona USA

Funder

National Institute of Neurological Disorders and Stroke

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.a.62930

Reference4 articles.

1. Variability in Cerebral Palsy Diagnosis

2. Molecular Diagnostic Yield of Exome Sequencing in Patients With Cerebral Palsy

3. A report: The definition and classification of cerebral palsy April 2006;Rosenbaum P.;Developmental Medicine and Child Neurology. Supplement,2007

4. Trends in the Prevalence of Autism Spectrum Disorder, Cerebral Palsy, Hearing Loss, Intellectual Disability, and Vision Impairment, Metropolitan Atlanta, 1991–2010

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Potential clinical applications of advanced genomic analysis in cerebral palsy;eBioMedicine;2024-08

2. Cerebral Palsy Phenotypes in Genetic Epilepsies;Pediatric Neurology;2024-08

3. Redefining cerebral palsies as a diverse group of neurodevelopmental disorders with genetic aetiology;Nature Reviews Neurology;2023-08-03

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