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Type 2 Gaucher Disease with Hydrops Fetalis in an Ashkenazi Jewish Family Resulting from a Novel Recombinant Allele and a Rare Splice Junction Mutation in the Glucocerebrosidase Locus

✍ Scribed by K. Reissner; N. Tayebi; B.K. Stubblefield; V. Koprivica; M. Blitzer; W. Holleran; T. Cowan; S. Almashanu; A. Maddalena; E.M. Karson; E. Sidransky


Book ID
115639370
Publisher
Elsevier Science
Year
1998
Tongue
English
Weight
649 KB
Volume
63
Category
Article
ISSN
1096-7192

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