Results 21 to 30 of about 12,757,608 (345)

Child care licensing and regulation: A Key Topic Resource List [PDF]

open access: yes, 2006
A compilation of selected Research Connections resources focused on child care licensing and regulation, covering the areas of regulatory policies and practices, and the relationship of licensing to quality of care, child outcomes, and child care and ...
Child Care & Early Education Research Connections
core   +1 more source

The Long-Run Impacts of a Universal Child Care Program

open access: yesAmerican Economic Journal: Economic Policy, 2019
Past research documents the persistence of positive impacts of early life interventions on noncognitive skills. We test the symmetry of this finding by studying the persistence of a sizeable negative shock to noncognitive outcomes arising with the ...
Michael Baker   +2 more
semanticscholar   +1 more source

Who Benefits from Universal Child Care? Estimating Marginal Returns to Early Child Care Attendance

open access: yesJournal of Political Economy, 2018
We examine heterogeneous treatment effects of a universal child care program in Germany by exploiting variation in attendance caused by a reform that led to a large expansion staggered across municipalities.
T. Cornelissen   +3 more
semanticscholar   +1 more source

Child care licensing and regulation: A Key Topic Resource List [PDF]

open access: yes, 2010
A compilation of selected Research Connections resources focused on child care licensing and regulation, covering the areas of regulatory policies and practices, and the relationship of licensing to quality of care, child outcomes, and both child care ...
Child Care & Early Education Research Connections
core   +1 more source

Xp11.22 duplications in four unrelated Chinese families: delineating the genotype-phenotype relationship for HSD17B10 and FGD1

open access: yesBMC Medical Genomics, 2020
Background Xp11.22 duplications have been reported to contribute to nonsyndromic intellectual disability (ID). The HUWE1 gene has been identified in all male Xp11.22 duplication patients and is associated with nonsyndromic ID.
Qingming Wang   +5 more
doaj   +1 more source

Child care subsidy administration: A Key Topic Resource List [PDF]

open access: yes, 2011
A compilation of selected Research Connections resources focused on the administration of child care subsidy and Temporary Assistance to Needy Families (TANF) programs, including resources on the coordination of child care subsidy and TANF administration,
Child Care & Early Education Research Connections
core   +1 more source

Maternal substance use and child protection: a rapid evidence assessment of factors associated with loss of child care.

open access: yesInternational Journal of Child Abuse & Neglect, 2017
This article reviews the literature on the factors associated with mothers who use substances losing care of their children. A rapid evidence assessment was conducted in accordance with the Preferred Reporting Items for Systematic Reviews and Meta ...
M. Canfield   +4 more
semanticscholar   +1 more source

Child care decision-making: a Key Topic Resource List [PDF]

open access: yes, 2009
A compilation of selected Research Connections resources focused on the child care choices of parents with young children, including a summary of issues addressed in the literature, and a list of resources in the areas of choices associated with ...
Child Care & Early Education Research Connections
core   +1 more source

Subsidized child care and quality: A Key Topic Resource List [PDF]

open access: yes, 2014
A compilation of selected Research Connections resources focused on subsidized child care and quality, including a summary of issues addressed in the literature and a listing of resources about the relationships among child care subsidies, program ...
Child Care & Early Education Research Connections
core   +1 more source

Concurrent pathogenic variants in SLC6A1/NOTCH1/PRIMPOL genes in a Chinese patient with myoclonic-atonic epilepsy, mild aortic valve stenosis and high myopia

open access: yesBMC Medical Genetics, 2020
Background Pathogenic SLC6A1 variants have been reported in patients with myoclonic-atonic epilepsy (MAE). NOTCH1, encoding a member of the Notch family of proteins, is known to be associated with aortic valve disease.
Haiming Yuan   +5 more
doaj   +1 more source

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