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Werner syndrome: studies in an affected family reveal a cellular phenotype of unaffected siblings

✍ Scribed by Harald G. Weirich; Helga Weirich-Schwaiger; Heinz Kofler; Alexis Sidoroff; Peter Fritsch; Dietrich O. Schachtschabel; Manfred Schweiger; Monica Hirsch-Kauffmann


Book ID
116084932
Publisher
Elsevier Science
Year
1996
Tongue
English
Weight
976 KB
Volume
88
Category
Article
ISSN
0047-6374

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