Publication Date
In 2025 | 0 |
Since 2024 | 0 |
Since 2021 (last 5 years) | 0 |
Since 2016 (last 10 years) | 0 |
Since 2006 (last 20 years) | 3 |
Descriptor
Genetics | 3 |
Infant Care | 3 |
Screening Tests | 3 |
Child Health | 2 |
Neonates | 2 |
Access to Health Care | 1 |
Access to Information | 1 |
At Risk Persons | 1 |
Barriers | 1 |
Case Studies | 1 |
Computer Software Reviews | 1 |
More ▼ |
Source
Mental Retardation and… | 3 |
Author
Fomous, Cathy | 1 |
Mann, Marie | 1 |
Miller, Naomi | 1 |
Puryear, Michele | 1 |
Strickland, Bonnie | 1 |
Watson, Michael | 1 |
Watson, Michael S. | 1 |
Weissman, Gloria | 1 |
van Dyck, Peter C. | 1 |
Publication Type
Journal Articles | 3 |
Reports - Descriptive | 3 |
Education Level
Elementary Secondary Education | 3 |
Higher Education | 3 |
Adult Education | 1 |
Early Childhood Education | 1 |
Audience
Location
Laws, Policies, & Programs
Assessments and Surveys
What Works Clearinghouse Rating
Puryear, Michele; Weissman, Gloria; Watson, Michael; Mann, Marie; Strickland, Bonnie; van Dyck, Peter C. – Mental Retardation and Developmental Disabilities Research Reviews, 2006
Newborn screening and genetic technologies are expanding and changing rapidly, increasing the demand for genetic specialty services. Because of the scarcity and geographic maldistribution of genetic specialty services, access to these services is a critical issue. This article discusses some of the efforts initiated by the Maternal and Child…
Descriptors: Child Health, Genetics, Neonates, Infant Care
Watson, Michael S. – Mental Retardation and Developmental Disabilities Research Reviews, 2006
Newborn screening is considered a highly successful public health program that has resulted in the reduction of mortality, mental retardation, and other serious disabilities in thousands of children since the introduction of screening for phenylketonuria (PKU) in the 1960s. Programs are based in state public health departments such that each state…
Descriptors: Health Programs, Public Health, Child Health, Genetics
Fomous, Cathy; Miller, Naomi – Mental Retardation and Developmental Disabilities Research Reviews, 2006
Expanded newborn screening programs and subsequent detection of rare genetic disorders challenge parents and their medical providers to learn about the treatment and management of these disorders. Many people seek medical information on the Internet but may encounter requests for registration or fees, or find that resources are out of date,…
Descriptors: Genetic Disorders, Genetics, Government Libraries, Library Role