← Evidence map

ArticleHuman genetics2017

Exome analysis of Smith-Magenis-like syndrome cohort identifies de novo likely pathogenic variants.

Seth I Berger et al.PubMed ↗Full text ↗Publisher ↗

No numbers read from the abstract.

20 papers cite it

2017
2018
2019
2020
2021
2022
2023
2024
2025
2026
this papercites it
Full record →Abstract, authors, funding and every citing paper · PMID 28213671