「Xeroderma」の共起表現(1語右で並び替え)

Xeroderma pigmentosum has an autosomal recessive patte

Additionally, there is a relationship with xeroderma pigmentosum in that virtually all PIBI(D)S p

XPB ( Xeroderma Pigmentosum B) is an ATP dependent human DNA

use loss of this gene results in the disease Xeroderma Pigmentosum Variant.

haracterized by the skin and eye symptoms of xeroderma pigmentosum (XP) occurring in association wi

genetic mutations of NER proteins including Xeroderma pigmentosum and Cockayne's syndrome.

The most common defect in xeroderma pigmentosum is an autosomal recessive geneti

1, 2, 3 (which is itself is associated with Xeroderma Pigmentosum) and type 4).

from the rare (but real) disease called XP ( xeroderma pigmentosum).

occurs when an individual also suffers from Xeroderma pigmentosum, another DNA repair disease.

ads to a number of genetic disorders such as Xeroderma Pigmentosum, Cockayne's syndrome, and Tricho

Amane, a 17-year-old girl, who suffers from Xeroderma pigmentosum, forbid her to going out during

in a rare autosomal recessive disease called xeroderma pigmentosum.

「Xeroderma」の共起表現一覧(1語右で並び替え)