The University of Chicago Header Logo

Connection

William Dobyns to Chromosomes, Human, Pair 22

This is a "connection" page, showing publications William Dobyns has written about Chromosomes, Human, Pair 22.
Connection Strength

0.476
  1. Polymicrogyria and deletion 22q11.2 syndrome: window to the etiology of a common cortical malformation. Am J Med Genet A. 2006 Nov 15; 140(22):2416-25.
    View in: PubMed
    Score: 0.294
  2. Cerebellar and posterior fossa malformations in patients with autism-associated chromosome 22q13 terminal deletion. Am J Med Genet A. 2013 Jan; 161A(1):131-6.
    View in: PubMed
    Score: 0.112
  3. Description of a new oncogenic mechanism for atypical teratoid rhabdoid tumors in patients with ring chromosome 22. Am J Med Genet A. 2017 Jan; 173(1):245-249.
    View in: PubMed
    Score: 0.037
  4. Lissencephaly and other malformations of cortical development: 1995 update. Neuropediatrics. 1995 Jun; 26(3):132-47.
    View in: PubMed
    Score: 0.033
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.