Construct · 1 fields · 1 citations

contiguous gene syndrome: a standalone construct

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contiguousgene syndrome1 CONSTRUCTContiguous gene syndromeSCHMICKEL · MEDICAL GENETICS

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Medical genetics

a recognizable syndrome caused by deletion or duplication of several adjacent genes, each contributing part of the combined phenotype.

In medical genetics, contiguous gene syndrome refers to a recognizable syndrome caused by deletion or duplication of several adjacent genes, each contributing part of the combined phenotype. This meaning comes from Schmickel (1986) in The Journal of Pediatrics.[1]

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Nearby constructs

phenotype4 fields · 4 citationsjingle · one word, four constructssyndrome3 fields · 3 citationsjingle · one word, three constructs

References

  1. Schmickel, R. D. (1986). Contiguous gene syndromes: A component of recognizable syndromes. The Journal of Pediatrics, 109(2), 231-241. https://doi.org/10.1016/s0022-3476(86)80377-8

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