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Springer Publishing Company

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A locus for juvenile myoclonic epilepsy maps to 2q33–q36

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A Newly Identified Locus for Usher Syndrome Type I, USH1E, Maps to Chromosome 21q21

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DFNB44, a Novel Autosomal Recessive Non-Syndromic Hearing Impairment Locus, Maps to Chromosome 7p14.1-q11.22

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A new locus for autosomal dominant Charcot-Marie-Tooth disease type 2 (CMT2L) maps to chromosome 12q24

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Human Genetics, Vol. 114, Iss. 6, 2004-05 ,pp. : 527-533

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