← Evidence map

ArticleJournal of medical genetics2006

Identification of a recurrent breakpoint within the SHANK3 gene in the 22q13.3 deletion syndrome.

M C Bonaglia et al.PubMed ↗Full text ↗Publisher ↗

No numbers read from the abstract.

92 papers cite itlatest 60 shown

2006
…
2012
2013
2014
2015
2016
2017
2018
2019
2021
2022
2023
2024
2025
this paperpooled ittrialcites it
Full record →Abstract, authors, funding and every citing paper · PMID 16284256