Papers: 10.1186/s12887-020-02309-0
https://doi.org/10.1186/s12887-020-02309-0
Concurrent OPA1 mutation and chromosome 3q deletion leading to Behr syndrome: a case report
Cited by: 2
Author(s): Ting Zeng, Linyan Liao, Yi Guo, Xuxu Liu, Xuejian Xiong, Yu Zhang, Shi Cen, Honghui Li, Shuzhang Wei
Published: almost 5 years ago
Software Mentions 1
pypi: CNVkit
Copy number variation toolkit for high-throughput sequencing.Papers that mentioned: 161
Very Likely Science (65)