Prenatal diagnosis of Batten's disease
Author:
Publisher
Elsevier BV
Subject
General Medicine
Reference9 articles.
1. Neuronal ceroid lipofuscinoses in childhood;Santavuori;Brain Dev,1989
2. Batten diease (Spielmeyer-Vogt disease, juvenile onset neuronal ceroid lipofuscinosis) gene (CLN3) maps to human chromosome 16;Gardiner;Genomics,1990
3. Genetic mapping of the Batten disease locus (CLN3) to the interval D16S288-D16S383 by analysis of haplotypes and allelic association;Mitchison;Genomics,1994
4. Isolation of a novel gene underlying Batten disease (CLN3);The International Batten disease Consortium;Cell,1995
5. Prenatal diagnosis of the infantile type of neuronal ceroid lipofuscinosis by electron microscopic investigation of human chorionic villi;Rapola;Prenat Diagn,1990
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1. Recent Insight into the Genetic Basis, Clinical Features, and Diagnostic Methods for Neuronal Ceroid Lipofuscinosis;International Journal of Molecular Sciences;2022-05-20
2. Therapeutic landscape for Batten disease: current treatments and future prospects;Nature Reviews Neurology;2019-02-19
3. Batten Disease;Encyclopedia of Special Education;2014-02-07
4. Bioinformatic perspectives in the neuronal ceroid lipofuscinoses;Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease;2013-11
5. Prenatal Diagnosis of Disorders of Lipid Metabolism;Genetic Disorders and the Fetus;2010-09-24
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