← Evidence map

ArticleClinical case reports2019

Familial segregation of a 5q15-q21.2 deletion associated with facial dysmorphism and speech delay.

Cinthya Zepeda-Mendoza et al.PubMed ↗Full text ↗Publisher ↗

No numbers read from the abstract.

5 papers cite it

2019
2020
2021
2022
2023
2024
this papercites it
Full record →Abstract, authors, funding and every citing paper · PMID 31183085