[Report of siblings with xeroderma pigmentosum, genetic complementation group D].
1985
Y Mitoh, and
Y Satoh, and
M Kobayashi, and
A Kawada, and
Y Fujiwara
UI
MeSH Term
Description
Entries
D008297
Male
Males
D002648
Child
A person 6 to 12 years of age. An individual 2 to 5 years old is CHILD, PRESCHOOL.
Children
D002675
Child, Preschool
A child between the ages of 2 and 5.
Children, Preschool,Preschool Child,Preschool Children
D005260
Female
Females
D005816
Genetic Complementation Test
A test used to determine whether or not complementation (compensation in the form of dominance) will occur in a cell with a given mutant phenotype when another mutant genome, encoding the same mutant phenotype, is introduced into that cell.
Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D014983
Xeroderma Pigmentosum
A rare, pigmentary, and atrophic autosomal recessive disease. It is manifested as an extreme photosensitivity to ULTRAVIOLET RAYS as the result of a deficiency in the enzyme that permits excisional repair of ultraviolet-damaged DNA.
Kaposi Disease,Kaposi's Disease,Kaposis Disease
Related Publications
Y Mitoh, and
Y Satoh, and
M Kobayashi, and
A Kawada, and
Y Fujiwara