Prenatal diagnosis for de novo mutations: Experience from a tertiary center over a 10‐year period

BACKGROUND: This study summarizes the results of prenatal diagnosis due to a history of de novo mutation in a previous pregnancy, in a tertiary center in Israel, over a 10‐year period. METHODS: We sorted all cases of de novo mutations from a pool of 2,260 pregnancies for which prenatal molecular dia...

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Sparad:
Bibliografiska uppgifter
I publikationen:Mol Genet Genomic Med
Huvudupphovsmän: Eyal, Ori, Berkenstadt, Michal, Reznik‐Wolf, Haike, Poran, Hana, Ziv‐Baran, Tomer, Greenbaum, Lior, Yonath, Hagit, Pras, Elon
Materialtyp: Artigo
Språk:Inglês
Publicerad: John Wiley and Sons Inc. 2019
Ämnen:
Original Articles
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC6465671/
https://ncbi.nlm.nih.gov/pubmed/30693677
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mgg3.573
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