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 (47338)
CDC/NIH Web Information Database (32125)
CDC-Authored Genomics and Precision Health Publications Database (5555)
Precision Health Database (63390)
Tier-Classified Guidelines Database (532)
Pathogen Advanced Molecular Detection Database (26591)
All of Us Reports and Publications Database (634)
Human Genome Epidemiology
Human Genome Epidemiology Literature Finder (225926)
Epigenetic Epidemiology Publications Database (22563)
Release Note
Contact Us
Precision Health Database
Precision Health Database|Search|Public Health Genomics and Precision Health Knowledge Base (PHGKB)
Last data update: Mar 28, 2024
. (Total: 63390 Documents since 2012)
All
Cancer
Diabetes
Economic
Environmental
Equity
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 - 20 (of 20 Records)
Query Trace:
Prenatal testing[original query]>>Guidelines Related[Product Type]
Noninvasive prenatal screening (NIPS) for fetal chromosome abnormalities in a general-risk population: An evidence-based clinical guideline of the American College of Medical Genetics and Genomics (ACMG)
JS Dungan et al, Genetics in Medicine, December 16, 2022
[Progress of research on clinical use of non-invasive prenatal screening for special groups of pregnant women].
Yan Yousheng et al. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2021 38(7) 694-698
Similar articles in PubMed
Screening for autosomal recessive and X-linked conditions during pregnancy and preconception: a practice resource of the American College of Medical Genetics and Genomics (ACMG).
Gregg Anthony R et al. Genetics in medicine : official journal of the American College of Medical Genetics 2021
Similar articles in PubMed
Direct-to-consumer prenatal testing for multigenic or polygenic disorders: a position statement of the American College of Medical Genetics and Genomics (ACMG)
ACMG Board of Directors, Genetics in Medicine, June 28, 2021
Screening for Fetal Chromosomal Abnormalities: ACOG Practice Bulletin Summary, Number 226.
et al. Obstetrics and gynecology 2020 Oct 136(4) 859-867
Similar articles in PubMed
Committee Opinion No. 406: Prenatal testing after IVF with preimplantation genetic testing for aneuploidy.
Zwingerman Rhonda et al. Journal of obstetrics and gynaecology Canada : JOGC = Journal d'obstetrique et gynecologie du Canada : JOGC 2020 Aug
Similar articles in PubMed
The use of fetal exome sequencing in prenatal diagnosis: a points to consider document of the American College of Medical Genetics and Genomics (ACMG)
KG Monaghan et al. Genetics in Medicine, January 8, 2020
Practice guideline: joint CCMG-SOGC recommendations for the use of chromosomal microarray analysis for prenatal diagnosis and assessment of fetal loss in Canada.
Armour Christine M et al. Journal of medical genetics 2018 Mar
Similar articles in PubMed
Assessing the cost of implementing the 2011 Society of Obstetricians and Gynecologists of Canada and Canadian College of Medical Genetics practice guidelines on the detection of fetal aneuploidies.
Lilley Margaret et al. Prenatal diagnosis 2017 Jul
Similar articles in PubMed
Recommended practice for laboratory reporting of non-invasive prenatal testing (NIPT) of trisomies 13, 18 and 21: a consensus opinion.
Deans Zandra C et al. Prenatal diagnosis 2017 May
Similar articles in PubMed
Non-invasive Prenatal Testing: Exploring ethical issues in biology and medicine
Nuffeld Bioethics Report, March 2017
Noninvasive prenatal screening for fetal aneuploidy, 2016 update: a position statement of the American College of Medical Genetics and Genomics.
Gregg Anthony R et al. Genetics in medicine : official journal of the American College of Medical Genetics 2016 Jul
Similar articles in PubMed
Prenatal Testing for Adult-Onset Conditions: the Position of the National Society of Genetic Counselors.
Hercher Laura et al. Journal of genetic counseling 2016 Jul
Similar articles in PubMed
Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening. Summary and recommendations.
Dondorp Wybo et al. Eur. J. Hum. Genet. 2015 Apr 1.
Similar articles in PubMed
Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening.
Dondorp Wybo et al. Eur. J. Hum. Genet. 2015 Mar 18.
Similar articles in PubMed
EMQN best practice guidelines for the molecular genetic testing and reporting of fragile X syndrome and other fragile X-associated disorders.
Similar articles in PubMed
Offering prenatal diagnostic tests: European guidelines for clinical practice [corrected].
Similar articles in PubMed
Position Statement from the Italian College of Fetal Maternal Medicine: Non-invasive prenatal testing (NIPT) by maternal plasma DNA sequencing.
Similar articles in PubMed
NSGC practice guideline: prenatal screening and diagnostic testing options for chromosome aneuploidy.
Similar articles in PubMed
Noninvasive prenatal testing/noninvasive prenatal diagnosis: the position of the National Society of Genetic Counselors.
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:
Mar 28, 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