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Human Molecular Genetics, Vol. 6, Iss. 1, 1997-01 ,pp. : 17-26

Oxford University Press

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Dopa-Responsive Dystonia in British Patients: New Mutations of the GTP-Cyclohydrolase I Gene and Evidence for Genetic Heterogeneity

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Hereditary lymphedema: evidence for linkage and genetic heterogeneity

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Human Molecular Genetics, Vol. 7, Iss. 13, 1998-12 ,pp. : 2073-2078

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Mapping of the Familial Infantile Myasthenia (Congenital Myasthenic Syndrome Type Ia) Gene to Chromosome 17p with Evidence of Genetic Homogeneity

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A Candidate Gene Association Study Further Corroborates Involvement of Contactin Genes in Autism

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Karger

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