14 ????? 2017 xeroderma pigmentosum oculodermal melanocytosis
Xeroderma pigmentosum. A human disorder caused by defects in genes that encode proteins involved in global genome nucleotide excision repair (GG-NER). It is.
4 ???? 2008 tary diseases such as xeroderma pigmento- sum and non-polyposis colon cancer as well ... Xeroderma pigmentosum is a rare.
Xeroderma pigmentosum (XP) is a condition inherited as an autosomal recessive trait and is characterized by photosensitivity pigmentary changes
Xeroderma pigmentosum. (XPA-G). Bloom's syndrome. (BLM). 1st mutation. 2nd mutation 3rd mutation nth mutation. CANCER normal cells malignant cells.
derived from individuals with xeroderma pigmentosum which suggests that ionizing radiation of nucleotide-excision repair (xeroderma pigmentosum group.
https://www.uniklinik-duesseldorf.de/fileadmin/Fuer-Patienten-und-Besucher/Kliniken-Zentren-Institute/Institute/Zentralinstitut_fuer_Klinische_Chemie_und_Laboratoriumsdiagnostik/Lehre/Wahlpflichtk/Geronto/Literatur/WPK_Geronto_DNA_Damage_Hoeijmakers2009.pdf
25 ????? 2019 xeroderma pigmentosum complementation group G; XPF
Hereditary hemorrhagic telengiectasia syndrome. 6. Genodermatoses with malignant potential. • Xeroderma pigmentosum. • Dyskeratosis congenita
22 ????? 2014 Xeroderma pigmentosum (XP). ? Ataxia-telangiectasia (ATM). ? Fanconi pancytopenia. ? Hereditary dysplastic nevus syndrome.