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Autosomal recessive disease that is characterized by a deficiency in the ability to repair ultraviolet damage that has material basis in autosomal recessive inheritance of DNA repair.
I have xerodermapigmentosum-XPfor short- arareand frequently fatal genetic disorder.
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More extraordinary than surviving twenty-eight years unscathed by xerodermapigmentosum.
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Deficiencies in NER are associated with the extremely skin cancer-prone inherited disorder xerodermapigmentosum.
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Most physicians familiar with xerodermapigmentosum would have expected me to die in childhood.
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Ethan had XP, xerodermapigmentosum, an incredibly rare inherited disease that left him extremely sensitive to the sun's ultraviolet rays.
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Taking place amid the clean, whitewashed walls of Nicolas-on-the-Sparks, the story concerns an attractive, feisty teenager with a miraculously forgiving version of xerodermapigmentosum.
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Xerodermapigmentosum, first described by Kaposi in 1870, is a very rare disease, but owing to its striking peculiarities is easily recognized.
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Xerodermapigmentosum (XP) is a human disorder which is characterized by hypersensitivity to sunlight and elevated incidence of skin cancer.
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Xerodermapigmentosum (XP) is a rare disorder characterized by a high skin sun-sensitivity predisposing to skin cancers at an early age.