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Connection

Janet Poole to Founder Effect

This is a "connection" page, showing publications Janet Poole has written about Founder Effect.
Connection Strength

0,095
  1. Endocrine profiling in patients with Fanconi anemia, homozygous for a FANCG founder mutation. Mol Genet Genomic Med. 2020 08; 8(8):e1351.
    View in: PubMed
    Score: 0,044
  2. Phenotypic consequences in black South African Fanconi anemia patients homozygous for a founder mutation. Genet Med. 2014 May; 16(5):400-6.
    View in: PubMed
    Score: 0,028
  3. A common Fanconi anemia mutation in black populations of sub-Saharan Africa. Blood. 2005 May 01; 105(9):3542-4.
    View in: PubMed
    Score: 0,015
  4. Comparative study of Fanconi anemia in children of different ethnic origin in South Africa. Am J Med Genet. 1994 Sep 01; 52(3):279-84.
    View in: PubMed
    Score: 0,007
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.