Skip directly to search
Skip directly to A to Z list
Skip directly to navigation
Skip directly to page options
Skip directly to site content
Start of Search Controls
Search Form Controls
Search The CDC
submit
CDC A-Z Index
MENU
CDC A-Z
SEARCH
A
B
C
D
E
F
G
H
I
J
K
L
M
N
O
P
Q
R
S
T
U
V
W
X
Y
Z
#
Search Form Controls
Search The CDC
submit
CDC A-Z Index
Public Health Genomics and Precision Health Knowledge Base (v9.0)
PHGKB
About
Public Health Genomics Branch
PHGKB Weekly Horizon Scan
Genomics Precision Health Scan
Advanced Molecular Detection Clips
Non-Genomics Precision Health Scan
CDC-authored Publications Scan
Specialized PHGKB
Cancer PHGKB
Diabetes PHGKB
Economic Evaluation PHGKB
Environmental Health PHGKB
Family Health History PHGKB
Health Equity PHGKB
HLBS-PopOmics
Infectious Diseases PHGKB
Implementation Science PHGKB
Neurological Disorders PHGKB
Pharmacogenomics PHGKB
Primary Immune Deficiency Diseases PHGKB
Rare Diseases PHGKB
Reproductive and Child Health PHGKB
All Databases
COVID-19 GPH (47360)
CDC/NIH Web Information Database (32189)
CDC-Authored Genomics and Precision Health Publications Database (6062)
Precision Health Database (63767)
Tier-Classified Guidelines Database (534)
Pathogen Advanced Molecular Detection Database (26823)
All of Us Reports and Publications Database (675)
Human Genome Epidemiology
Human Genome Epidemiology Literature Finder (226691)
Epigenetic Epidemiology Publications Database (22811)
Release Note
Contact Us
Precision Health Database
Precision Health Database|Search|Public Health Genomics and Precision Health Knowledge Base (PHGKB)
Last data update: May 02, 2024
. (Total: 63767 Documents since 2012)
All
Cancer
Diabetes
Economic
Equity
Environmental
FHH
HLBS
ID
Implementation
ND
PGx
PI
Rare
RCH
dataset
All
GPH
Non-GPH
Filtered By
:
Select to fine-tune your search
Disease
Gene
Product Type
Category
Year
Previous
Records 1 - 30 (of 727 Records)
Next
Query Trace:
International Perspectives of Extended Genetic Sequencing When Used as Part of Newborn Screening to Identify Cystic Fibrosis.
Corinna C A Clark et al. Int J Neonatal Screen 2024 10(2)
Similar articles in PubMed
Cystic fibrosis newborn screening in Switzerland - evaluation and scenarios for improvement after 11 years of follow-up.
Esl Pedersen et al. J Cyst Fibros 2024
Similar articles in PubMed
Diagnosing Cystic Fibrosis in the 21st Century-A Complex and Challenging Task.
Dana-Teodora Anton-Paduraru et al. Diagnostics (Basel) 2024 14(7)
Similar articles in PubMed
Cystic Fibrosis Foundation Evidence-Based Guideline for the Management of CRMS/CFSPID.
Deanna M Green et al. Pediatrics 2024
Similar articles in PubMed
Prevalence of common autosomal recessive mutation carriers in women in the Southern Vietnam following the application of expanded carrier screening.
Xuan-Hong To-Mai et al. Sci Rep 2024 14(1) 7461
Similar articles in PubMed
Development of a Low Cost Semiquantitative Polymerase Chain Reaction Assay for Molecular Diagnosis of Williams Syndrome.
Dinali M Ranaweera et al. Clin Lab 2024 70(3)
Similar articles in PubMed
[Cystic fibrosis in Morroco : what do words mean without action ?].
Naima Amenzoui et al. Rev Med Liege 2024 79(3) 175-180
Similar articles in PubMed
ECFS standards of care on CFTR-related disorders: Towards a comprehensive program for affected individuals.
E De Wachter et al. J Cyst Fibros 2024
Similar articles in PubMed
Stakeholder Views of the Proposed Introduction of Next Generation Sequencing into the Cystic Fibrosis Screening Protocol in England.
Pru Holder et al. Int J Neonatal Screen 2024 10(1)
Similar articles in PubMed
The Psychological Impact on Parents of Children who Receive an Inconclusive Diagnosis for Cystic Fibrosis following Newborn Screening: A Systematic Mini-Review.
Ioanna Loukou et al. Children (Basel) 2024 11(1)
Similar articles in PubMed
Cystic Fibrosis Cases Missed by Newborn Bloodspot Screening-Towards a Consistent Definition and Data Acquisition.
Anne Munck et al. Int J Neonatal Screen 2023 9(4)
Similar articles in PubMed
The new face of cystic fibrosis in the era of population genetic carrier screening.
Miri Dotan et al. J Cyst Fibros 2023
Similar articles in PubMed
Outcome data from 15 years of cystic fibrosis newborn screening in a large UK region.
Sarah Jane Driscoll et al. Arch Dis Child 2023
Similar articles in PubMed
Cystic Fibrosis.
Hartmut Grasemann et al. N Engl J Med 2023 389(18) 1693-1707
Similar articles in PubMed
Effectiveness of preconceptional and prenatal cystic fibrosis carrier screening: a systematic review.
Rita Banzi et al. Epidemiol Prev 2023 47(4-5) 243-256
Similar articles in PubMed
Prospects for Expansion of Universal Newborn Screening in Bulgaria: A Survey among Medical Professionals.
Georgi Iskrov et al. Int J Neonatal Screen 2023 9(4)
Similar articles in PubMed
Every CFTR variant counts - Target-capture based next-generation-sequencing for molecular diagnosis in the German CF Registry.
Simone Ahting et al. J Cyst Fibros 2023
Similar articles in PubMed
The past 10 years of cystic fibrosis treatment: the road to cure.
Claudio Castaños et al. Lancet Respir Med 2023 11(10) 864-865
Similar articles in PubMed
[Comparison of diagnostic data after introduction of cystic fibrosis screening in newborns in Germany].
Lutz Nährlich et al. Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz 2023
Similar articles in PubMed
Standards for the care of people with cystic fibrosis (CF): A timely and accurate diagnosis.
Carlo Castellani et al. J Cyst Fibros 2023
Similar articles in PubMed
Performance of single-gene noninvasive prenatal testing for autosomal recessive conditions in a general population setting.
Julia Wynn et al. Prenat Diagn 2023
Similar articles in PubMed
A retrospective study on newborn screening for metabolic disorders.
Karam Chandrajit Singh et al. Bioinformation 2023 18(12) 1122-1125
Similar articles in PubMed
Optimization of performance of Dutch newborn screening for cystic fibrosis.
M J Bouva et al. J Cyst Fibros 2023
Similar articles in PubMed
Diagnostic challenges in CFTR-related metabolic syndrome: Where the guidelines fall short.
Erin F Kallam et al. Paediatr Respir Rev 2023
Similar articles in PubMed
Carrier Screening Programs for Cystic Fibrosis, Fragile X Syndrome, Hemoglobinopathies and Thalassemia, and Spinal Muscular Atrophy: A Health Technology Assessment.
et al. Ont Health Technol Assess Ser 2023 23(4) 1-398
Similar articles in PubMed
Experiences of cystic fibrosis newborn screening and genetic counseling.
Kimberly Foil et al. J Community Genet 2023
Similar articles in PubMed
Evaluation of newborn screening in the state of Mato Grosso from 2005 to 2019.
Roseli Divino Costa et al. Rev Paul Pediatr 2023 42e2022161
Similar articles in PubMed
Why cystic fibrosis newborn screening programs have failed to meet original expectations… thus far.
Philip M Farrell et al. Mol Genet Metab 2023 107679
Similar articles in PubMed
Children with cystic fibrosis are still receiving inconclusive diagnosis despite undergoing newborn screening.
Ioanna Loukou et al. Acta Paediatr 2023
Similar articles in PubMed
Use of genome sequencing to hunt for cryptic second-hit variants: analysis of 31 cases recruited to the 100 000 Genomes Project.
A Rachel Moore et al. J Med Genet 2023
Similar articles in PubMed
File Formats Help:
How do I view different file formats (PDF, DOC, PPT, MPEG) on this site?
Adobe PDF file
Microsoft PowerPoint file
Microsoft Word file
Microsoft Excel file
Audio/Video file
Apple Quicktime file
RealPlayer file
Text file
Zip Archive file
SAS file
ePub file
Page last reviewed:
Feb 1, 2024
Page last updated:
May 02, 2024
Content source:
Public Health Genomics Branch in the Division of Blood Disorders and Public Health Genomics
,
National Center on Birth Defects and Developmental Disabilities
TOP