← Evidence map

ArticleEuropean journal of human genetics : EJHG2019

Exome sequencing of fetal anomaly syndromes: novel phenotype-genotype discoveries.

Nicole Meier et al.PubMed ↗Full text ↗Publisher ↗

No numbers read from the abstract.

35 papers cite it

2019
2020
2021
2022
2023
2024
2025
2026
this paperpooled itcites it
Full record →Abstract, authors, funding and every citing paper · PMID 30679815