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Public Health Genomics and Precision Health Knowledge Base (v9.0)
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Precision Health Database|Search|Public Health Genomics and Precision Health Knowledge Base (PHGKB)
Reproductive and Child Health
Last data update: Mar 28, 2024
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Records 1 - 13 (of 13 Records)
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Dyslexia Or Learning Disability[original query]>>Original Studies[Product Type]
Long-term predictors of developmental outcome and disease burden in SCN1A-positive Dravet syndrome.
Tony Feng et al. Brain Commun 2024 6(1) fcae004
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"We are not a typical family anymore": Exploring the experiences and support needs of fathers of children with Fragile X syndrome in Australia.
Jacintha Luermans et al. Am J Med Genet A 2023
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Auditory phoneme discrimination, articulation, and language disorders in patients with genetic epilepsy with febrile seizures plus: A case-control study.
Sager Gunes et al. Epilepsy & behavior : E&B 2022 129108626
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Risks of covid-19 hospital admission and death for people with learning disability: population based cohort study using the OpenSAFELY platform.
Williamson Elizabeth J et al. BMJ (Clinical research ed.) 2021 374n1592
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Fast screening for children's developmental language disorders via comprehensive speech ability evaluation-using a novel deep learning framework.
Zhang Xing et al. Annals of translational medicine 2020 Jun 8(11) 707
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Prenatal exome sequencing analysis in fetal structural anomalies detected by ultrasonography (PAGE): a cohort study.
Lord Jenny et al. Lancet (London, England) 2019 Jan
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Impact of IQ on the diagnostic yield of chromosomal microarray in a community sample of adults with schizophrenia.
Lowther Chelsea et al. Genome medicine 2017 Nov 9(1) 105
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Understanding the health economic burden of patients with tuberous sclerosis complex (TSC) with epilepsy: a retrospective cohort study in the UK Clinical Practice Research Datalink (CPRD).
Shepherd Charles et al. BMJ open 2017 Oct 7(10) e015236
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Development and validation of QDiabetes-2018 risk prediction algorithm to estimate future risk of type 2 diabetes: cohort study.
Hippisley-Cox Julia et al. BMJ (Clinical research ed.) 2017 Nov 359j5019
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CNVs affecting cancer predisposing genes (CPGs) detected as incidental findings in routine germline diagnostic chromosomal microarray (CMA) testing.
Innes Josie et al. Journal of medical genetics 2017 Sep
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A scoping study to explore the cost-effectiveness of next-generation sequencing compared with traditional genetic testing for the diagnosis of learning disabilities in children.
Beale Sophie et al. Health technology assessment (Winchester, England) 2015 Jun 19(46) 1-90
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High acceptance of an early dyslexia screening test involving genetic analyses in Germany.
Wilcke Arndt et al. Eur. J. Hum. Genet. 2015 Jun 3.
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Cost Effectiveness of Using Array-CGH for Diagnosing Learning Disability.
Sagoo G S et al. Appl Health Econ Health Policy 2015 Apr 19.
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Page last reviewed:
Feb 1, 2024
Page last updated:
Mar 28, 2024
Content source:
Public Health Genomics Branch in the Division of Blood Disorders and Public Health Genomics
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National Center on Birth Defects and Developmental Disabilities
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