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Connection

YISHAY BEN MOSHE to Heterotaxy Syndrome

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This is a "connection" page, showing publications YISHAY BEN MOSHE has written about Heterotaxy Syndrome.
YISHAY BEN MOSHE
Connection Strength
0.179
Heterotaxy Syndrome
  1. Whole-exome sequencing reveals a monogenic cause in 56% of individuals with laterality disorders and associated congenital heart defects. J Med Genet. 2022 07; 59(7):691-696.
    View in: PubMed
    Score: 0.179
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.