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Connection

Katalin Csiszar to Chromosomes, Human, Pair 7

This is a "connection" page, showing publications Katalin Csiszar has written about Chromosomes, Human, Pair 7.
Connection Strength

0.050
  1. Urb?n Z, Helms C, Fekete G, Csisz?r K, Bonnet D, Munnich A, Donis-Keller H, Boyd CD. 7q11.23 deletions in Williams syndrome arise as a consequence of unequal meiotic crossover. Am J Hum Genet. 1996 Oct; 59(4):958-62.
    View in: PubMed
    Score: 0.037
  2. Pujana MA, Nadal M, Gratac?s M, Peral B, Csiszar K, Gonz?lez-Sarmiento R, Sumoy L, Estivill X. Additional complexity on human chromosome 15q: identification of a set of newly recognized duplicons (LCR15) on 15q11-q13, 15q24, and 15q26. Genome Res. 2001 Jan; 11(1):98-111.
    View in: PubMed
    Score: 0.013
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.
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