software mutation surveyor version 3.23 (SoftGenetics)
90
Structured Review
SoftGenetics
software mutation surveyor version 3.23
Software Mutation Surveyor Version 3.23, supplied by SoftGenetics, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/software+programme/software+programme+mutation+surveyor+v+3+30/pmc03004862-64-3-7
Average 90 stars, based on 1 article reviews
Software Mutation Surveyor Version 3.23, supplied by SoftGenetics, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/software+programme/software+programme+mutation+surveyor+v+3+30/pmc03004862-64-3-7
Average 90 stars, based on 1 article reviews
software mutation surveyor version 3.23 - by Bioz Stars,
2026-10
90/100 stars
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other:Article Title: High-Resolution Array CGH Profiling Identifies Na/K Transporting ATPase Interacting 2 (NKAIN2) as a Predisposing Candidate Gene in Neuroblastoma Article Snippet: Sequence data were analyzed via Article Title: Functional null mutations in the gonosomal homologue gene TBL1Y are associated with non-syndromic coarctation of the aorta. Article Snippet: In patients with congenital heart defects, chromosomal anomalies are 100 times more frequent than in control subjects.. Coarctation of the aorta can be detected in 15-20% of patients with Ullrich-Turner syndrome.. By extensively reviewing literature involving breakpoint analysis of gonosomal deletions in UllrichTurner syndrome patients with and without coarctation of the aorta, we identified several gonosomal homolgous gene pairs of interest. Article Title: Evaluation of genotype–phenotype relationships in patients referred for endocrine assessment in suspected Pendred syndrome Article Snippet: The data were collated using Foundation Data Collection v3.0 and were analysed using the software Software:Article Title: Mutations in SCG10 Are Not Involved in Hirschsprung Disease Article Snippet: Direct sequencing of exons 1–5 was performed using the 3730 DNA Analyser (Applied Biosystems). .. Using the software Mutagenesis:Article Title: Mutations in SCG10 Are Not Involved in Hirschsprung Disease Article Snippet: Direct sequencing of exons 1–5 was performed using the 3730 DNA Analyser (Applied Biosystems). .. Using the software |