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Phenocopy

A phenotypic trait or disease that resembles the trait expressed by a particular genotype, but in an individual who is not a carrier of that genotype… 
National Institutes of Health

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Phenotype

Papers overview

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Highly Cited
2012
Highly Cited
2012
Down‐regulated miR‐625 suppresses invasion and metastasis of gastric cancer by targeting ILK
2008
2008
A Hypomorphic Allele of Aryl Hydrocarbon Receptor-Associated Protein-9 Produces a Phenocopy of the Ahr-Null Mouse
The aryl hydrocarbon receptor-associated protein-9 (ARA9) is a chaperone of the aryl hydrocarbon receptor (AHR). The AHR has been… 
Review
2007
Review
2007
Retinoids and cardiovascular developmental defects
Vitamin A and related retinoids are critical regulators of normal cardiovascular development. Extreme variations in retinoid… 
2001
2001
A morpholino phenocopy of the cyclops mutation
Mutations of the cyclops locus produce a characteristic pattern of abnormalities, including prechordal plate and notochord… 
1999
1999
A segregation study of panic disorder in families of panic patients responsive to the 35% CO2 challenge
Highly Cited
1997
Highly Cited
1997
Vitamin K deficiency embryopathy: a phenocopy of the warfarin embryopathy due to a disorder of embryonic vitamin K metabolism.
Three unrelated infants presented with radiographic punctate calcifications, nasal hypoplasia, and abnormalities of the spine… 
1989
1989
A dominant phenocopy of hypopituitarism in transgenic mice resulting from central nervous system synthesis of human growth hormone.
We have produced a line of transgenic mice in which expression of human GH has been detected only in the cerebral cortex. Both… 
1977
1977
Dilution of hypoxanthine-guanine phosphoribosyl transferase and other factors affecting the frequency of 6-thioguanine resistance in Chinese hamster lung cells.
1970
1970
Allopurinol and xanthine nephropathy.
Treatment with allopurinol results in an induced xanthinuria. Allopurinol inhibits xanthine oxidase, the enzyme that catalyzes… 
Highly Cited
1966
Highly Cited
1966
Neurological Defect: Manganese in Phenocopy and Prevention of a Genetic Abnormality of Inner Ear
A specific congenital ataxia may be caused by presence of mutant genes and by manganese deficiency during prenatal development in… 
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