In-house genetic counseling increases the detection of abnormal karyotypes—a 26-year experience in prenatal diagnosis in a single tertiary referral hospital in Poland

PURPOSE: To evaluate the trends in prenatal diagnosis over 26 years in a tertiary referral hospital. METHODS: A retrospective analysis of invasive prenatal procedures performed between 1991 and 2016. Maternal characteristics, indications for invasive diagnosis, and percentage of abnormal karyotypes...

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Detalles Bibliográficos
Autores principales: Bijok, Julia, Kucińska–Chahwan, Anna, Massalska, Diana, Ilnicka, Alicja, Panek, Grzegorz, Roszkowski, Tomasz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2020
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7468017/
https://www.ncbi.nlm.nih.gov/pubmed/32424735
http://dx.doi.org/10.1007/s10815-020-01812-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7468017/
https://www.ncbi.nlm.nih.gov/pubmed/32424735
http://dx.doi.org/10.1007/s10815-020-01812-8

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