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D.P.1.12 FSHD and Williams syndrome: The occurrence of two genetic disorders due to heterozygous DNA fragment deletions in the same patient

✍ Scribed by G.L. Vita; M. Romano; S. Sinicropi; L. Colantone; A. Toscano; G. Vita; C. Rodolico


Book ID
116793443
Publisher
Elsevier Science
Year
2008
Tongue
English
Weight
49 KB
Volume
18
Category
Article
ISSN
0960-8966

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