Search Genetics: guidelines
Results 1 - 10 of 11
Search Results
Description:
These guidelines are designed to assist the pediatrician in caring for the child in whom the diagnosis of Down syndrome has been confirmed by karyotype. Although the pediatrician’s initial contact with the child is usually during infancy, occasionally the pregnant woman who has been given the prenatal diagnosis of Down syndrome will be referred for counseling. Therefore, these guidelines offer advice for this situation as well. (From Their Website)
Source:
AAP 0
Your rating: None
Description:
Newborn screening for congenital hypothyroidism: recommended guidelines
Source:
AAP 0
Your rating: None
Description:
National Guideline Clearinghouse is a public resource for evidence-based clinical practice guidelines. Users may start a search by typing keywords into the search box, or using the NGC Browse or Detailed Search features.
Source:
National Guideline Clearinghouse 0
Your rating: None
Tags:
Description:
Recommendations for Standards for Interpretation of Sequence Variations
Source:
ACMG 0
Your rating: None
Description:
Clinical trials for the research of Autism.
Source:
ClinicalTrials.gov 0
Your rating: None
Description:
Newborn screening has long been recognized as an essential, life-saving, and effective preventive public health service that has identified thousands of babies each year in the United States who are born with a genetic or metabolic disorder. In many cases, detecting these disorders spells the difference between life and death for these babies; in other instances, identifying newborns with a disorder means that they can be treated and thus not face life-long disability or cognitive impairment. Now, with the advent of new screening technology, babies can be tested—and treated— for many more disorders than was possible in the past. (From Their Website)
Source:
CDC 0
Your rating: None
Description:
Maternal serum screening has been modified during the past 25 years and is now widely utilized during the second trimester to identify women at risk for fetal open neural tube defects (ONTDs), anencephaly, and trisomies 21 and 18. This statement replaces the 1994 and 1996 ACMG position statements on serum screening and discusses clinical guidelines for screening that complement the sections of ACMG’s Standards and Guidelines for Clinical Genetics Laboratories entitled “Prenatal Screening for Open Neural Tube Defects” and “Prenatal Screening for Down Syndrome” (http://www.acmg.net). (From Their Website)
Source:
ACMG 0
Your rating: None
Description:
NBDPN Guidelines for Conducting Birth Defects Surveillance
Source:
NBDPN 0
Your rating: None
Description:
Statement on Universal Newborn Hearing Screening.
Source:
ACMG 0
Your rating: None
Description:
The mission of the National Institute of General Medical Sciences (NIGMS) is to support research that increases understanding of life processes and lays the foundation for advances in disease diagnosis, treatment, and prevention. NIGMS-funded researchers seek to answer important scientific questions in fields such as cell biology, biophysics, genetics, developmental biology, pharmacology, physiology, biological chemistry, bioinformatics, computational biology, selected aspects of the behavioral sciences, and specific cross-cutting clinical areas that affect multiple organ systems. NIGMS also provides leadership in training the next generation of scientists to assure the vitality and continued productivity of the research enterprise. (From Their Website)
Source:
National Institute of General Medical Sciences 0
Your rating: None
Add A Resource
Do you have a website or resource that should be included on our site?
Current search
[×]
Tags
: guidelinesGuided search
Click a term to refine your current search.
Resource Type
- practice guidelines (6)
- journal article (2)
- misc information materials (2)
- organization (1)
Tags
: all » guidelinesTopics
- genetic medical research (8)
- genetic testing (3)
- abnormalities (1)
- screening and diagnosis (1)