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Connection

SHWETA DHAR to Ectodermal Dysplasia

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This is a "connection" page, showing publications SHWETA DHAR has written about Ectodermal Dysplasia.
SHWETA DHAR
Connection Strength
0.301
Ectodermal Dysplasia
  1. Heterozygous MAP3K20 variants cause ectodermal dysplasia, craniosynostosis, sensorineural hearing loss, and limb anomalies. Hum Genet. 2024 Mar; 143(3):279-291.
    View in: PubMed
    Score: 0.208
  2. WDR35 mutation in siblings with Sensenbrenner syndrome: a ciliopathy with variable phenotype. Am J Med Genet A. 2012 Nov; 158A(11):2917-24.
    View in: PubMed
    Score: 0.094
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.