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Precision Health Database


Genomics & Health Impact Scan Database|Search|PHGKB

Rare Diseases

Last data update: Mar 28, 2023. (Total: 58963 Documents since 2012)
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Records 1 - 8 (of 8 Records)

Query Trace: Fragile X Syndrome[original query]>>Evidence Synthesis [Product Type]
Economic evaluation of population-based expanded reproductive carrier screening for genetic diseases in Australia.
Deborah Schofield et al. Genetics in medicine : official journal of the American College of Medical Genetics 2023 100813
Research Gaps in Fragile X Syndrome: An Updated Literature Review to Inform Clinical and Public Health Practice.
Raspa Melissa et al. Journal of developmental and behavioral pediatrics : JDBP 2022
Population genomic screening of all young adults in a health-care system: a cost-effectiveness analysis.
Zhang Lei et al. Genetics in medicine : official journal of the American College of Medical Genetics 2019 Feb
Fragile X checklists: A meta-analysis and development of a simplified universal clinical checklist.
Lubala Toni Kasole et al. Molecular genetics & genomic medicine 2018 Apr
Public Health Literature Review of Fragile X Syndrome.
Raspa Melissa et al. Pediatrics 2017 Jun 139(Suppl 3) S153-S171
Assessing the Fragile X Syndrome Newborn Screening Landscape.
Riley Catharine et al. Pediatrics 2017 Jun 139(Suppl 3) S207-S215
Developmental and behavioral pediatricians' attitudes toward screening for fragile X.
Genetic counseling and testing for FMR1 gene mutations: practice guidelines of the national society of genetic counselors.
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