[Answer to the article by F. Vialrd et al.: 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]. / Réponse à l'article de F. Vialard et al. : la prévalence des microdélétions et microduplications pathogènes récurrentes en diagnostic prénatal doit-elle amener à revoir l'évolution des techniques de dépistage non invasif ? L'exemple de la région 22q11.2.
Gynecol Obstet Fertil Senol
; 45(1): 50-53, 2017 01.
Article
em Fr
| MEDLINE
| ID: mdl-28238318
Palavras-chave
Texto completo:
1
Coleções:
01-internacional
Base de dados:
MEDLINE
Assunto principal:
Diagnóstico Pré-Natal
/
Deleção Cromossômica
Tipo de estudo:
Diagnostic_studies
/
Prevalence_studies
/
Risk_factors_studies
/
Screening_studies
Limite:
Female
/
Humans
/
Pregnancy
Idioma:
Fr
Revista:
Gynecol Obstet Fertil Senol
Ano de publicação:
2017
Tipo de documento:
Article