Connection

VERNON SUTTON to Uniparental Disomy

This is a "connection" page, showing publications VERNON SUTTON has written about Uniparental Disomy.
Connection Strength

0.429
  1. Skeletal defects in paternal uniparental disomy for chromosome 14 are re-capitulated in the mouse model (paternal uniparental disomy 12). Hum Genet. 2003 Oct; 113(5):447-51.
    View in: PubMed
    Score: 0.213
  2. Allele-specific methylation of a functional CTCF binding site upstream of MEG3 in the human imprinted domain of 14q32. Chromosome Res. 2005; 13(8):809-18.
    View in: PubMed
    Score: 0.063
  3. Epigenetic detection of human chromosome 14 uniparental disomy. Hum Mutat. 2003 Jul; 22(1):92-7.
    View in: PubMed
    Score: 0.053
  4. Comprehensive microsatellite marker analysis contradicts previous report of segmental maternal heterodisomy of chromosome 14. J Med Genet. 2003 Mar; 40(3):e26.
    View in: PubMed
    Score: 0.052
  5. The importance of investigating for uniparental disomy in prenatally identified balanced acrocentric rearrangements. Prenat Diagn. 2002 Feb; 22(2):141-3.
    View in: PubMed
    Score: 0.048
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.