Connection

WILLIAM CRAIGEN to Genetic Linkage

This is a "connection" page, showing publications WILLIAM CRAIGEN has written about Genetic Linkage.
Connection Strength

0.086
  1. Revised fine mapping of the human voltage-dependent anion channel loci by radiation hybrid analysis. Mamm Genome. 1999 Oct; 10(10):1041-2.
    View in: PubMed
    Score: 0.037
  2. Autosomal recessive Noonan syndrome associated with biallelic LZTR1 variants. Genet Med. 2018 10; 20(10):1175-1185.
    View in: PubMed
    Score: 0.033
  3. Mutation and expression analysis of the endoglin gene in hereditary hemorrhagic telangiectasia reveals null alleles. Hum Mutat. 1998; 11(4):286-94.
    View in: PubMed
    Score: 0.008
  4. A submicroscopic deletion in Xq26 associated with familial situs ambiguus. Am J Hum Genet. 1997 Aug; 61(2):395-401.
    View in: PubMed
    Score: 0.008
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.