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[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
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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