[Does the prevalence of recurrent pathogenic microdeletions and microdoublements in prenatal diagnosis lead to a reassessment of the evolution of non-invasive screening techniques? The example of region 22q11.2]

Subjects

Subjects :

Heart Defects, Congenital
Phenotype
Pregnancy
Chromosomes, Human, Pair 22
Prenatal Diagnosis
DiGeorge Syndrome
Prevalence
Humans
Female
Chromosome Deletion
Gene Deletion
In Situ Hybridization, Fluorescence

Details

Language :

French

ISSN :

24687189

Volume :

45

Issue :

1

Database :

OpenAIRE

Journal :

Gynecologie, obstetrique, fertilitesenologie

Accession number :

edsair.pmid..........e0bc70d24eddeb521fdd7bda75696829