Huifang Yan
4PUBLICATIONS
17CO-AUTHORS
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Publications (4)
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|Sep 09, 2022
The recurrent mutation in RNF220 also causes hypomyelination in China and is a CpG hot spot.Huifang Yan, Thomas Kubisiak, Kai Gao
|Feb 10, 2022
Genome sequencing demonstrates high diagnostic yield in children with undiagnosed global developmental delay/intellectual disability: A prospective study.Yu Sun, Jing Peng, Desheng Liang
|Feb 18, 2021
Genetic analysis of 20 patients with hypomyelinating leukodystrophy by trio-based whole-exome sequencing.Huifang Yan, Haoran Ji, Thomas Kubisiak
|Jun 03, 2020
A second cohort of CHD3 patients expands the molecular mechanisms known to cause Snijders Blok-Campeau syndrome.Theodore G Drivas, Dong Li, Divya Nair
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Frequent Collaborators
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Tahsin Stefan Barakat
1 joint publications
Patrick R Blackburn
1 joint publications
Margit Burmeister
1 joint publications
Gregory M Cooper
1 joint publications
Alejandro Ferrer
1 joint publications
Zoe Powis
1 joint publications
Francesca Clementina Radio
1 joint publications
Kristen J Rasmussen
1 joint publications
Erica D Smith
1 joint publications
Thomas Smol
