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Connection

Carole Ober to Genetic Diseases, Inborn

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This is a "connection" page, showing publications Carole Ober has written about Genetic Diseases, Inborn.
Carole Ober
Connection Strength
0.089
Genetic Diseases, Inborn
  1. Exome sequencing reveals a novel mutation for autosomal recessive non-syndromic mental retardation in the TECR gene on chromosome 19p13. Hum Mol Genet. 2011 Apr 01; 20(7):1285-9.
    View in: PubMed
    Score: 0.089
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.