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Prenatal Diagnosis of Wilson's Disease by Analysis of DNA Polymorphism
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Homing in on Wilson's Disease
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Association of HTRA1 Mutations and Familial Ischemic Cerebral Small-Vessel Disease
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Strong Clustering and Stereotyped Nature of Notch3 Mutations, in CADASIL Patients
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Molecular Genetics in Neurology
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Central Nervous System Lesions in von Hippel-Lindau Syndrome
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Retinitis Pigmentosa
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