The mutational spectrum of human malignant autosomal recessive osteopetrosis

By Chitayat D.  

Human Molecular Genetics, Vol. 10, Iss. 17, 2001-08 ,pp. : 1767-1773

Oxford University Press

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Localization of a Gene Responsible for Autosomal Recessive Demyelinating Neuropathy with Focally Folded Myelin Sheaths to Chromosome 11q23 by Homozygosity Mapping and Haplotype Sharing

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Human Molecular Genetics, Vol. 5, Iss. 7, 1996-01 ,pp. : 1051-1054

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Homozygosity Mapping of an Autosomal Recessive Form of Demyelinating Charcot-Marie-Tooth Disease to Chromosome 5q23–q33

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Human Molecular Genetics, Vol. 5, Iss. 10, 1996-10 ,pp. : 1685-1688

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Autosomal recessive nonsyndromic deafness locus DFNB63 at chromosome 11q13.2–q13.3

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Mapping of DFNB12 , a Gene for a Non-Syndromal Autosomal Recessive Deafness, to Chromosome 10q21–22

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Human Molecular Genetics, Vol. 5, Iss. 7, 1996-01 ,pp. : 1061-1064

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