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C8 deficiency in a family with xeroderma pigmentosum: Lack of linkage to the HLA region

✍ Scribed by G. Giraldo; L. Degos; E. Beth; M. Sasportes; A. Marcelli; R. Gharbi; Noorbibi K. Day


Book ID
118373290
Publisher
Elsevier Science
Year
1977
Tongue
English
Weight
478 KB
Volume
8
Category
Article
ISSN
1090-2341

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Linkage analysis in a family with the Op
✍ May, Melanie; Huston, Sara; Wilroy, R. Sid; Schwartz, Charles πŸ“‚ Article πŸ“… 1997 πŸ› John Wiley and Sons 🌐 English βš– 486 KB πŸ‘ 2 views

The Opitz GBBB syndrome (OS) is characterized in part by widely spaced inner ocular canthi and hypospadias. Recently, linkage analysis showed that the gene for the X-linked form to be located in an 18 cM region spanning Xp22. We have now conducted linkage analysis in a family previously published as