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Publications by Michel Koenig

Homozygosity Mapping of Portuguese and Japanese Forms of Ataxia-Oculomotor Apraxia to 9p13, and Evidence for Genetic Heterogeneity

American Journal of Human Genetics
Genetics
2001English

Homozygosity Mapping of Spinocerebellar Ataxia With Cerebellar Atrophy and Peripheral Neuropathy to 9q33–34, and With Hearing Impairment and Optic Atrophy to 6p21–23

European Journal of Human Genetics
Genetics
2000English

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