Papers: 10.3390/diagnostics10050286
https://doi.org/10.3390/diagnostics10050286
Whole Exome Sequencing with Comprehensive Gene Set Analysis Identified a Biparental-Origin Homozygous c.509G>A Mutation in PPIB Gene Clustered in Two Taiwanese Families Exhibiting Fetal Skeletal Dysplasia during Prenatal Ultrasound
Cited by: 7
Author(s): Ting‐Yu Chang, I‐Fang Chung, Wan‐Ju Wu, Shun‐Ping Chang, Wen‐Hsiang Lin, Norman Ginsberg, Gwo‐Chin Ma, Ming Chen
Published: over 6 years ago
Software Mentions 2
Very Likely Science (60)
pypi: fasta
The fasta python package enables you to deal with biological sequence files easily.Papers that mentioned: 848
Very Likely Science (80)