U.S. newborn screening policy dilemmas for the twenty-first century.
about
Newborn screening for cystic fibrosis: a lesson in public health disparitiesTracking clinical genetic services for newborns identified through newborn dried bloodspot screening in the United States-lessons learnedGenetics Evaluation Guidelines for the Etiologic Diagnosis of Congenital Hearing Loss. Genetic Evaluation of Congenital Hearing Loss Expert Panel. ACMG statementPresent status and future concerns of expanded newborn screening in malaysia: sustainability, challenges and perspectivesCurrent situation and prospects of newborn screening and treatment for Phenylketonuria in China - compared with the current situation in the United States, UK and Japan.Population genetic screening programmes: principles, techniques, practices, and policies.Determining the effect of newborn hearing screening legislation: an analysis of state hearing screening rates.Perceptions Regarding Importance and Skill at Policy Development Among Public Health StaffNewborn screening and the obstetrician.The Impact of the Affordable Care Act on Funding for Newborn Screening Services.Web-based newborn screening system for metabolic diseases: machine learning versus clinicians.Screening and outcomes in biliary atresia: summary of a National Institutes of Health workshop.Policy Making in Newborn Screening Needs a Structured and Transparent Approach.International differences in the evaluation of conditions for newborn bloodspot screening: a review of scientific literature and policy documents.Questioning the Need for Informed Consent: A Case Study of California's Experience with a Pilot Newborn Screening Research Project.State Legislation, Regulations, and Hospital Guidelines for Newborn Screening for Critical Congenital Heart Defects - United States, 2011-2014.Genetic susceptibility to aminoglycoside ototoxicity: how many are at risk?Assuring clinical genetic services for newborns identified through U.S. newborn screening programs.Newborn screening program for hemoglobinopathies in Rio de Janeiro, Brazil.Randomized comparison of phone versus in-person BRCA1/2 predisposition genetic test result disclosure counseling.Newborn screening for developmental disabilities: reframing presumptive benefit.Newborn screening: complexities in universal genetic testing.
P2860
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P2860
U.S. newborn screening policy dilemmas for the twenty-first century.
description
2001 nî lūn-bûn
@nan
2001 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
name
U.S. newborn screening policy dilemmas for the twenty-first century.
@ast
U.S. newborn screening policy dilemmas for the twenty-first century.
@en
U.S. newborn screening policy dilemmas for the twenty-first century.
@nl
type
label
U.S. newborn screening policy dilemmas for the twenty-first century.
@ast
U.S. newborn screening policy dilemmas for the twenty-first century.
@en
U.S. newborn screening policy dilemmas for the twenty-first century.
@nl
prefLabel
U.S. newborn screening policy dilemmas for the twenty-first century.
@ast
U.S. newborn screening policy dilemmas for the twenty-first century.
@en
U.S. newborn screening policy dilemmas for the twenty-first century.
@nl
P356
P1476
U.S. newborn screening policy dilemmas for the twenty-first century.
@en
P2093
Therrell BL Jr
P356
10.1006/MGME.2001.3238
P577
2001-09-01T00:00:00Z