The University of Chicago Header Logo

Connection

Robert Wollmann to Phenotype

This is a "connection" page, showing publications Robert Wollmann has written about Phenotype.
Connection Strength

0.081
  1. Rapsyn mutations in myasthenic syndrome due to impaired receptor clustering. Muscle Nerve. 2003 Sep; 28(3):293-301.
    View in: PubMed
    Score: 0.035
  2. Histopathologic changes in the extraocular muscle in centronuclear myopathy with a Dynamin 2 mutation. Ophthalmic Genet. 2013 Mar-Jun; 34(1-2):83-6.
    View in: PubMed
    Score: 0.016
  3. Variable phenotypes associated with mutations in DOK7. Muscle Nerve. 2008 Apr; 37(4):448-56.
    View in: PubMed
    Score: 0.012
  4. Foamy cells with oligodendroglial phenotype in childhood ataxia with diffuse central nervous system hypomyelination syndrome. Acta Neuropathol. 2000 Dec; 100(6):635-46.
    View in: PubMed
    Score: 0.007
  5. Developmental expression of BPAG1-n: insights into the spastic ataxia and gross neurologic degeneration in dystonia musculorum mice. Dev Biol. 1997 Jul 15; 187(2):131-42.
    View in: PubMed
    Score: 0.006
  6. Gene targeting of BPAG1: abnormalities in mechanical strength and cell migration in stratified epithelia and neurologic degeneration. Cell. 1995 Apr 21; 81(2):233-43.
    View in: PubMed
    Score: 0.005
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.