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Mapping of the Choroideremia-like (CHML) Gene at 1q42-qter and Mutation Analysis in Patients with Usher Syndrome Type II

✍ Scribed by Hans v. Bokhoven; Carolien v. Genderen; Catherine M. Molloy; Dorien J.R. v.d. Pol; Cor W.R.J. Cremers; Annelies v. Aarem; Marianne Schwartz; Thomas Rosenberg; Ad H.M.Geurts v. Kessel; Hans Hilfiger Ropers; Frans P.M. Cremers


Book ID
115611944
Publisher
Elsevier Science
Year
1994
Tongue
English
Weight
209 KB
Volume
19
Category
Article
ISSN
0888-7543

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