Header Logo

Connection

Elizabeth Berry-Kravis to Base Sequence

This is a "connection" page, showing publications Elizabeth Berry-Kravis has written about Base Sequence.
Connection Strength

0.088
  1. New Pvu II mitochondrial polymorphism in a mother and son of Indian ancestry. Am J Med Genet. 1994 Oct 15; 53(1):94-6.
    View in: PubMed
    Score: 0.032
  2. Germline mosaicism of PHOX2B mutation accounts for familial recurrence of congenital central hypoventilation syndrome (CCHS). Am J Med Genet A. 2012 Sep; 158A(9):2297-301.
    View in: PubMed
    Score: 0.027
  3. Genetic variation in the HTR1A gene and sudden infant death syndrome. Am J Med Genet A. 2008 Apr 01; 146A(7):930-3.
    View in: PubMed
    Score: 0.020
  4. Methylation analysis of the fragile X syndrome by PCR. Genet Test. 1997-1998; 1(3):151-5.
    View in: PubMed
    Score: 0.009
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.