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Detection of RAG mutations and prenatal diagnosis in families presenting with either T–B– severe combined immunodeficiency or Omenn's syndrome

✍ Scribed by U Tabori; Z Mark; N Amariglio; A Etzioni; H Golan; B Biloray; A Toren; G Rechavi; I Dalal


Book ID
110887888
Publisher
John Wiley and Sons
Year
2004
Tongue
English
Weight
159 KB
Volume
65
Category
Article
ISSN
0009-9163

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