Construct · 1 fields · 1 citations

triallelic inheritance: a standalone construct

One name. One construct. A landmark on the map.

● anchor · a standalone construct Nearest construct by meaning·not indexed

A single standalone construct; nearby constructs are located against it in the Collider. Tap a field for its definition, unit, and measures.

Medical genetics

inheritance in which a recessive disorder shows full expression only when a third mutant allele at a second locus joins two mutant alleles at the first.

In medical genetics, triallelic inheritance refers to inheritance in which a recessive disorder shows full expression only when a third mutant allele at a second locus joins two mutant alleles at the first. This meaning comes from Katsanis (2001) in Science.[1]

Unit
Recovery means
Measured by

Run it through the Collider, or take the citations with you.

See how triallelic inheritance sits against neighbouring constructs in the Collider, or export every reference on this page in one click.

Open in Collider Export BibTeX Report this entry

Nearby constructs

allele3 fields · 5 citationsjingle · one word, three constructs expression4 fields · 4 citationsjingle · one word, four constructs inheritance3 fields · 4 citationsjingle · one word, three constructs

References

Katsanis, N., Ansley, S. J., Badano, J. L., Eichers, E. R., Lewis, R. A., Hoskins, B. E., Scambler, P. J., Davidson, W. S., Beales, P. L., & Lupski, J. R. (2001). Triallelic Inheritance in Bardet-Biedl Syndrome, a Mendelian Recessive Disorder. Science, 293(5538), 2256-2259. https://doi.org/10.1126/science.1063525

Cited on this page?

Confirm your construct, or correct us.

If your work is cited behind one of these entries, you know better than we do whether we captured the meaning right. Confirm it, suggest an edit, or dispute it, and your name goes on the entry as an author who has checked it, linked to your ORCID.

Claim your construct