[Array-comparative genomic hybridization is a new and promising method for prenatal chromosomal diagnosis]. / Array-komparativ genomisk hybridisering er en ny og lovende metode til prænatal kromosomundersøgelse .
Ugeskr Laeger
; 176(30): 1379-82, 2014 Jul 21.
Article
in Da
| MEDLINE
| ID: mdl-25292226
ABSTRACT
Array-comparative genomic hybridization (array-CGH) is a very sensitive method for identifying chromosomal imbalances and is now used on a clinical basis for prenatal diagnosis. This article reviews the advantages and disadvantages of the method, the ethical considerations and the current recommendations for prenatal use in Denmark according to a new national guideline from The Danish Society of Foetal Medicine and the Danish Society of Medical Genetics.
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Collection:
01-internacional
Database:
MEDLINE
Main subject:
Prenatal Diagnosis
/
Chromosome Disorders
/
Comparative Genomic Hybridization
Type of study:
Diagnostic_studies
/
Guideline
/
Prognostic_studies
Limits:
Female
/
Humans
/
Pregnancy
Language:
Da
Journal:
Ugeskr Laeger
Year:
2014
Type:
Article