Genetic and clinical aspects of X-linked hydrocephalus (L1 disease): Mutations in theL1CAMgene
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Reference89 articles.
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4. Neural cell recognition molecule L1: from cell biology to human hereditary brain malformations;Brümmendorf;Curr Opin Neurobiol,1998
5. Recurrence risk for congenital hydrocephalus;Burton;Clin Genet,1979
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