FARIDA ABID to INDEL Mutation
This is a "connection" page, showing publications FARIDA ABID has written about INDEL Mutation.
Connection Strength
0.040
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Clinical exome sequencing reveals locus heterogeneity and phenotypic variability of cohesinopathies. Genet Med. 2019 03; 21(3):663-675.
Score: 0.040
Connection Strength
The connection strength for concepts is the sum of the scores for each matching publication.
Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.