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Prenatal diagnosis of xeroderma pigmentosum (group C) using assays of unscheduled DNA synthesis and postreplication repair

✍ Scribed by D. J. J. Halley; W. Keijzer; N. G. J. Jaspers; M. F. Niermeuer; W. J. Rleijer; J. Boué; A. Boué; D. Bootsma

Book ID
119838843
Publisher
John Wiley and Sons
Year
2008
Tongue
English
Weight
574 KB
Volume
16
Category
Article
ISSN
0009-9163

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Useful applications of DNA repair tests
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✍ E. Ohtoshi; Y. Matsumura; C. Nishigori; K-I. Toda; Y. Horiguchi; M. Ikenaga; Y. 📂 Article 📅 2001 🏛 John Wiley and Sons 🌐 English ⚖ 564 KB

Dyschromatosis symmetrica hereditaria (DSH) is a hereditary skin disease characterized by the presence of pigmented and hypopigmented macules on the extremities and freckles on the face. However, if clinical features are not fully developed in infantile patients, it is difficult to differentiate DSH