Connection

DAVID NELSON to Translocation, Genetic

This is a "connection" page, showing publications DAVID NELSON has written about Translocation, Genetic.
Connection Strength

0.082
  1. Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome. Cell. 1991 May 31; 65(5):905-14.
    View in: PubMed
    Score: 0.033
  2. Allele-defined genome of the autopolyploid sugarcane Saccharum spontaneum L. Nat Genet. 2018 11; 50(11):1565-1573.
    View in: PubMed
    Score: 0.027
  3. Isolation of cDNA sequences around the chromosomal breakpoint in a female with Lowe syndrome by direct screening of cDNA libraries with yeast artificial chromosomes. J Inherit Metab Dis. 1992; 15(4):526-31.
    View in: PubMed
    Score: 0.017
  4. The Lowe's oculocerebrorenal syndrome gene encodes a protein highly homologous to inositol polyphosphate-5-phosphatase. Nature. 1992 Jul 16; 358(6383):239-42.
    View in: PubMed
    Score: 0.004
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.