Next Generation Sequencing Competence Network

Next Generation Sequencing Competence Network

e.g. CCGA
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Connection

Ingo Kurth to Ectromelia

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This is a "connection" page, showing publications Ingo Kurth has written about Ectromelia.
Ingo Kurth
Connection Strength
0,131
Ectromelia
  1. Duplications of BHLHA9 are associated with ectrodactyly and tibia hemimelia inherited in non-Mendelian fashion. J Med Genet. 2012 Feb; 49(2):119-25.
    View in: PubMed
    Score: 0,105
  2. Deletions in PITX1 cause a spectrum of lower-limb malformations including mirror-image polydactyly. Eur J Hum Genet. 2012 Jun; 20(6):705-8.
    View in: PubMed
    Score: 0,026
Connection Strength

The connection strength for topics 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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