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

By LeGuern E.   Guilbot A.   Kessali M.   Ravisé N.   Tassin J.   Maisonobe T.   Grid D.   Brice A.  

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

Oxford University Press

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

By Chaïb Hassan  

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

Oxford University Press

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Mutations in a new cytochrome P450 gene in lamellar ichthyosis type 3

By Lefèvre Caroline   Bouadjar Bakar   Ferrand Véronique   Tadini Gianluca   Mégarbané André   Lathrop Mark   Prud'homme Jean-François   Fischer Judith  

Human Molecular Genetics, Vol. 15, Iss. 5, 2006-03 ,pp. : 767-776

Oxford University Press

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A new locus for autosomal dominant amelogenesis imperfecta on chromosome 8q24.3

By Mendoza Gustavo   Pemberton Trevor   Lee Kwanghyuk   Scarel-Caminaga Raquel   Mehrian-Shai Ruty   Gonzalez-Quevedo Catalina   Ninis Vasiliki   Hartiala Jaana   Allayee Hooman   Snead Malcolm   Leal Suzanne   Line Sergio   Patel Pragna  

Human Genetics, Vol. 120, Iss. 5, 2007-01 ,pp. : 653-662

Springer Publishing Company

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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

By Bolino Alessandra  

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

Oxford University Press

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