P852: Prenatal whole genome sequencing to diagnosis rare presentations of hydrops fetalis

Authors

Corrine Nelson
Myra Wick (ORCID: https://orcid.org/0000-0003-4126-4523)
Laura Rust

Institutions

WinnMed (US)

Publication Details

Journal: Genetics in Medicine Open
Published: 2025-01-01
DOI: https://doi.org/10.1016/j.gimo.2025.103221
Primary Topic: Parvovirus B19 Infection Studies
Type: article
Field-Weighted Citation Impact: 0.00

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article

P852: Prenatal whole genome sequencing to diagnosis rare presentations of hydrops fetalis

Corrine Nelson, Myra Wick, Laura Rust

Jan 1, 2025

Genetics in Medicine Open

Parvovirus B19 Infection Studies

article

P852: Prenatal whole genome sequencing to diagnosis rare presentations of hydrops fetalis

Corrine Nelson, Myra Wick, Laura Rust

January 1, 2025article en

Abstract

No abstract available for this paper.

Genetics in Medicine OpenVol. 3

WinnMed (US)

Zero hunger

Openalex Percentile: Top 93%

Parvovirus B19 Infection Studies

DOI Open Access PDF OpenAlex

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P852: Prenatal whole genome sequencing to diagnosis rare presentations of hydrops fetalis — Corrine Nelson, Myra Wick, et al. · Genetics in Medicine Open (2025) | TGRS Research Map | TGRS